Liu, Lei et al. published their research in Archiv der Pharmazie (Weinheim, Germany) | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Recommanded Product: 4-Chlororesorcinol

Design, synthesis, and evaluation of novel 3,4-isoxazolediamide derivatives for the combination treatment of azole-resistant candidiasis was written by Liu, Lei;Sun, Yixiang;Gao, Zixuan;Yin, Wenbo;Jiang, Hong;Wu, Tianxiao;Sun, Yin;Qin, Qiaohua;Zhao, Dongmei;Cheng, Maosheng. And the article was included in Archiv der Pharmazie (Weinheim, Germany).Recommanded Product: 4-Chlororesorcinol The following contents are mentioned in the article:

Herein, the structural optimization and structure-activity relationship studies of 3,4-isoxazolediamide analogs I [R1 = 4-FC6H4, 3-isoxazole, benzo(b)thien-2-yl, etc.] and II [R2 = NHMe, NH(i-Pr), NMe2, etc.] were reported. As a new class of fungal Hsp90 inhibitor, compound I [R1 = 5-(morpholinomethyl)isoxazol-3-yl] was found to have good synergistic effects with fluconazole and to avoid potential mammalian toxicity. It also showed remarkable metabolic stability in vitro. Collectively, compound I [R1 = 5-(morpholinomethyl)isoxazol-3-yl] could be a promising lead compound for drug discovery targeting fungal Hsp90 and deserves further investigation. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Recommanded Product: 4-Chlororesorcinol).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Recommanded Product: 4-Chlororesorcinol

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Macdonald, Emily K. et al. published their research in European Polymer Journal in 2017 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Electric Literature of C6H5ClO2

Aromatic polyphosphonates as high refractive index polymers was written by Macdonald, Emily K.;Lacey, Joseph C.;Ogura, Ichiro;Shaver, Michael P.. And the article was included in European Polymer Journal in 2017.Electric Literature of C6H5ClO2 The following contents are mentioned in the article:

Highly refractive and transparent polyphosphonates with varying aromatic backbones have been synthesized by polycondensation of phosphonic dichlorides and diols, significantly expanding the reported scope of these intrinsic high refractive index polymers. The polyphosphonates display excellent thermal properties, with thermal stability up to 450°C and tuneable glass transition temperatures ranging from 41 to 214°C by terminating the polymer with different alcs. The polymers synthesized also possess excellent optical properties, with low UV cut off points and high refractive indexes up to 1.66, the highest reported for this type of polymer. We also report Abbe numbers for this class of polymers for the first time; all are high (>22), making these polymers excellent potential candidates for a range of optical applications. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Electric Literature of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Electric Literature of C6H5ClO2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Chen, Hong-Ming et al. published their research in Carbohydrate Research in 2016 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Category: chlorides-buliding-blocks

Synthesis and evaluation of a series of 6-chloro-4-methylumbelliferyl glycosides as fluorogenic reagents for screening metagenomic libraries for glycosidase activity was written by Chen, Hong-Ming;Armstrong, Zachary;Hallam, Steven J.;Withers, Stephen G.. And the article was included in Carbohydrate Research in 2016.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

Screening of large enzyme libraries such as those derived from metagenomic sources requires sensitive substrates. Fluorogenic glycosides typically offer the best sensitivity but typically must be used in a stopped format to generate good signal. Use of fluorescent phenols of pKa < 7, such as halogenated coumarins, allows direct screening at neutral pH. The synthesis and characterization of a set of nine different glycosides of 6-chloro-4-methylumbelliferone are described. The use of these substrates in a pooled format for screening of expressed metagenomic libraries yielded a “hit rate” of 1 in 60. Hits were then readily deconvoluted with the individual substrates in a single plate to identify specific activities within each clone. The use of such a collection of substrates greatly accelerates the screening process. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Category: chlorides-buliding-blocks).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Category: chlorides-buliding-blocks

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Smolobochkin, A. V. et al. published their research in RSC Advances in 2017 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Electric Literature of C6H5ClO2

Tandem intramolecular cyclisation/1,3-aryl shift in N-(4,4-diethoxybutyl)-1-arylmethanimines (Kazan reaction): synthesis of 3-benzylidene-1-pyrrolines was written by Smolobochkin, A. V.;Gazizov, A. S.;Melyashova, A. S.;Voronina, J. K.;Strelnik, A. G.;Vatsadze, S. Z.;Burilov, A. R.;Pudovik, M. A.;Fedorova, O. A.;Sinyashin, O. G.. And the article was included in RSC Advances in 2017.Electric Literature of C6H5ClO2 The following contents are mentioned in the article:

In this article, a novel tandem reaction, which transformed N-(4,4-diethoxybutyl)imines into 3-arylidene-1-pyrrolines, was described. The substrate scope of the starting acetals included arenes with electron-donating and withdrawing groups. The X-ray study of products confirmed the E-stereochem. of the double bonds formed. The best yields (99%) were found in boiling xylene in the presence of TsOH (or 2-nitroresocinol) during 40 (50) hours. The study of substituents effect on the course of the reaction revealed that cascade process took place, combining acid-catalyzed intramol. cyclization of N-(4,4-diethoxybutyl)imines and unusual 1,3-sigmatropic shift of the aryl fragment. Cyclic imines that were formed in high/excellent yields were of interest both from the viewpoint of their biol. activity and synthetic usefulness. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Electric Literature of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Electric Literature of C6H5ClO2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Gungor, Tugba et al. published their research in Monatshefte fuer Chemie in 2020 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Application In Synthesis of 4-Chlororesorcinol

One pot, multicomponent protocol for the synthesis of novel imidazo[1,2-a]pyrimidine-based pyran analogs: a potential biological scaffold was written by Gungor, Tugba. And the article was included in Monatshefte fuer Chemie in 2020.Application In Synthesis of 4-Chlororesorcinol The following contents are mentioned in the article:

An efficient procedure between imidazo[1,2-a]pyrimidine-2-carbaldehyde, malononitrile, enolizable C-H activated acidic compounds, ROH (R = 3-hydroxyphenyl, 4-chloro-3-hydroxyphenyl, naphthalen-1-yl, etc.) dimedone and sodium carbonate is described for the synthesis of potential biol. active, novel imidazo[1,2-a]pyrimidine-based pyran analogs I (R1 = 7-OH, 6-Cl-7-OH, 7,8-CH=CHCH=CH) and II through one pot, multicomponent reactions at room temperature This method provided mild reaction conditions, simple purification without column chromatog., and moderate to good yields for the construction of imidazo[1,2-a]pyrimidine-based pyran derivatives I and II. The structures of target compounds were established with different spectroscopic analyses. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Application In Synthesis of 4-Chlororesorcinol).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Application In Synthesis of 4-Chlororesorcinol

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Fouda, Ahmed M. et al. published their research in Medicinal Chemistry Research in 2016 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.COA of Formula: C6H5ClO2

Synthesis of several 4H-chromene derivatives of expected antitumor activity was written by Fouda, Ahmed M.. And the article was included in Medicinal Chemistry Research in 2016.COA of Formula: C6H5ClO2 The following contents are mentioned in the article:

Multi-component reactions for the preparation of 4H-chromene derivatives under microwave irradiation from different aromatic aldehydes with a mixture of malononitrile and phenol derivatives were established. The cytotoxic activity of the target compounds was evaluated against four cancer cell lines MCF-7, HCT-116, HepG-2 and A549 in comparison with vinblastine and colchicine as reference drugs. Generally, several compounds showed good cell growth inhibitory activity as compared to standard drugs. The structure-activity relationship studies reported that the substitution at 4- and 6-positions in 4H-chromene nucleus with the specific halogen atom increases the ability of the mol. against the different cell lines. The structures of the synthesized compounds were established on the basis of spectral data, IR, 1H NMR, 13C NMR and MS data. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5COA of Formula: C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.COA of Formula: C6H5ClO2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Wang, Sha-sha et al. published their research in Huagong Sheji Tongxun in 2021 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.SDS of cas: 95-88-5

Analysis of monitoring results of 32 dyes in oxidized hair dyes was written by Wang, Sha-sha;Ren, Lian;Liao, Xue. And the article was included in Huagong Sheji Tongxun in 2021.SDS of cas: 95-88-5 The following contents are mentioned in the article:

Using the determination method of 32 components including p-phenylenediamine in the “Safety Tech. Specifications for Cosmetics” (2015 edition), 24 batches of com. available oxidized hair dyes were tested, and the test results, batch formulations, and label indications were tested. The quality of cosmetics on the market was compared and analyzed to provide tech. support for cosmetics supervision. The results showed that none of the 32 components were detected, 16 batches of samples had inconsistent test results and batch formula, accounting for 67%, and 16 batches of samples had inconsistent test results and labeling, accounting for 67%, 5 batches of samples had inconsistent batch formula and labeling, accounting for 21%, and there were 16 batches of problematic samples, and the failure rate was 67%. It is recommended that the standardized supervision of production enterprises should be strengthened. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5SDS of cas: 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.SDS of cas: 95-88-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Szymkowiak, Joanna et al. published their research in Chemistry – A European Journal in 2018 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.SDS of cas: 95-88-5

One-step Access to Resorcinsalens-Solvent-Dependent Synthesis, Tautomerism, Self-sorting and Supramolecular Architectures of Chiral Polyimine Analogues of Resorcinarene was written by Szymkowiak, Joanna;Warzajtis, Beata;Rychlewska, Urszula;Kwit, Marcin. And the article was included in Chemistry – A European Journal in 2018.SDS of cas: 95-88-5 The following contents are mentioned in the article:

Substituted 2,4- and 4,6-dihydroxyisophthalaldehydes were condensed with optically pure and racemic trans-1,2-diaminocyclohexane to form resorcinarene-like polyimine macrocycles (resorcinsalens), the structure and stoichiometry of which were controlled by the choice of the reaction medium. Particularly, the cyclocondensation reactions were driven by the solubility, tautomerization, or by social self-sorting. The resorcinsalens crystallized as inclusion compounds, in which the guest mols. were situated either in channels or in voids. In the highly hydrated crystals of one of the [2+2] macrocycles and chloroform-solvated crystals of a [4+4] product the channels were interconnected, as in zeolites, enabling possible migration of loosely bound solvent mols. in three dimensions. The association mode depended on the structural modification of the host mol. and the type of included solvent mol.(s). This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5SDS of cas: 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.SDS of cas: 95-88-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Li, Qing et al. published their research in Angewandte Chemie, International Edition in 2020 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Recommanded Product: 95-88-5

An Activatable Polymeric Reporter for Near-Infrared Fluorescent and Photoacoustic Imaging of Invasive Cancer was written by Li, Qing;Li, Shenhua;He, Shasha;Chen, Wan;Cheng, Penghui;Zhang, Yan;Miao, Qingqing;Pu, Kanyi. And the article was included in Angewandte Chemie, International Edition in 2020.Recommanded Product: 95-88-5 The following contents are mentioned in the article:

Discriminative detection of invasive and noninvasive breast cancers is crucial for their effective treatment and prognosis. However, activatable probes able to do so in vivo are rare. Herein, we report an activatable polymeric reporter (P-Dex) that specifically turns on near-IR (NIR) fluorescent and photoacoustic (PA) signals in response to the urokinase-type plasminogen activator (uPA) overexpressed in invasive breast cancer. P-Dex has a renal-clearable dextran backbone that is linked with a NIR dye caged with an uPA-cleavable peptide substrate. Such a mol. design allows P-Dex to passively target tumors, activate NIR fluorescence and PA signals to effectively distinguish invasive MDA-MB-231 breast cancer from noninvasive MCF-7 breast cancer, and ultimately undergo renal clearance to minimize the toxicity potential. Thus, this polymeric reporter holds great promise for the early detection of malignant breast cancer. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Recommanded Product: 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Recommanded Product: 95-88-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Liu, Zhiwei et al. published their research in Sensors and Actuators, B: Chemical in 2018 | CAS: 95-88-5

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Recommanded Product: 95-88-5

A FRET chemosensor for hypochlorite with large Stokes shifts and long-lifetime emissions was written by Liu, Zhiwei;Song, Fengling;Song, Bo;Jiao, Long;An, Jing;Yuan, Jingli;Peng, Xiaojun. And the article was included in Sensors and Actuators, B: Chemical in 2018.Recommanded Product: 95-88-5 The following contents are mentioned in the article:

A FRET-based chemosensor for hypochlorite was developed, both the donor and acceptor of this FRET system are fluorophores with a large Stokes shift. The donor has two comparable excitation peaks at 460 nm and 575 nm. And it is found FRET-sensitized emission has less interference from direct-excited acceptor emission when excitation at 460 nm compared with excitation at 575 nm. The sensitivity can be improved for 4-fold (<95 nM). Meanwhile the donor can be excited by two-photon excitation source, which is an anti-Stokes shift property. It makes the chemosensor totally to get rid of the direct-excited acceptor emission for the FRET sensing method. Furthermore, the long lifetime luminescence of the FRET pairs makes them possible to be used in time-resolved technol., this can overcome the autofluorescence interference from biol. matrix. All above characters implied this FRET pairs have more potential to be applied in hypochlorite detection of biol. samples. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Recommanded Product: 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Recommanded Product: 95-88-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics