Category: 95-88-5

The reactions of 2-ethoxyvinyldichlorophosphonate with 4-chloro- or 4-bromoresorcinols and 2,3,5-trimethylphenol was written by Sadikova, Larisa M.;Sadykova, Yulia M.;Zalaltdinova, Alena V.;Burilov, Alexander R.;Pudovik, Michael A.;Voronina, Julia K.;Mitrasov, Yuriy N.. And the article was included in Phosphorus, Sulfur and Silicon and the Related Elements in 2016.Application of 95-88-5 The following contents are mentioned in the article:

This paper presents the results of the reaction of 2-ethoxyvinyldichlorophosphonate with 4-chloro- or 4-bromoresorcinols and 2,3,5-trimethylphenol. The reactions were carried out in toluene in the presence of trifluoroacetic acid. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Application of 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Application of 95-88-5

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

Reaction of 9-[2-(1,3-dioxolan-2-yl)ethyl]-9H-purin-6-amine with phenols. Synthesis of diarylpropanes was written by Smolobochkin, A. V.;Gazizov, A. S.;Vagapova, L. I.;Burilov, A. R.;Bogdanov, A. A.;Pudovik, M. A.. And the article was included in Russian Journal of Organic Chemistry in 2017.Recommanded Product: 4-Chlororesorcinol The following contents are mentioned in the article:

New 1,1-diarylpropanes containing an adenine fragment on C³ have been synthesized by reaction of 9-[2-(1,3-dioxolan-2-yl)ethyl]-9H-purin-6-amine with phenols in aqueous HCl. 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 can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. 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.Recommanded Product: 4-Chlororesorcinol

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

Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment was written by Smolobochkin, A. V.;Yakhshilikova, L. J.;Bekrenev, D. D.;Gazizov, A. S.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of General Chemistry in 2022.Recommanded Product: 4-Chlororesorcinol The following contents are mentioned in the article:

Based on the acid-catalyzed reaction of functionalized aminoacetals with C-nucleophiles, a series of new diarylmethane derivatives with a taurine fragment were synthesized. 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 can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. 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

Acid-catalyzed reaction of 1-(2,2-dimethoxyethyl)ureas with phenols as an effective approach to diarylethanes and dibenzoxanthenes was written by Smolobochkin, A. V.;Gazizov, A. S.;Voronina, J. K.;Rizbayeva, T. S.;Burilov, A. R.;Pudovik, M. A.. And the article was included in ARKIVOC (Gainesville, FL, United States) in 2019.Formula: C6H5ClO2 The following contents are mentioned in the article:

A one-pot synthesis of urea-substituted diarylethanes and dibenzoxanthenes starting from 1-(2,2-dimethoxyethyl)ureas and phenols was developed. The approach used readily available reagents and catalysts, requires mild reaction conditions and provides the target compounds in good to high yields. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Formula: C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Formula: C6H5ClO2

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

Reaction of 4-Chloro-6-[1-(vinylsulfonyl)pyrrolidin-2-yl]benzene-1,3-diol with Some Amines was written by Smolobochkin, A. V.;Anikina, E. A.;Gazizov, A. S.;Vagapova, L. I.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of General Chemistry in 2018.Synthetic Route of C6H5ClO2 The following contents are mentioned in the article:

4-Chloro-6-[1-(vinylsulfonyl)pyrrolidin-2-yl]benzene-1,3-diol prepared by the reaction of 2-ethoxypyrrolidine with 4-chlororesorcinol was introduced into the aza-Michael reaction with various amines which led to the formation of new 1-sulfonyl-2-arylpyrrolidines. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Synthetic Route of C6H5ClO2).

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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Synthetic Route of C6H5ClO2

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

Wide temperature-range, multi-component, optically isotropic antiferroelectric bent-core liquid crystal mixtures for display applications was written by Wang, Junren;Bergquist, Leah;Hwang, Jung-Im;Kim, Kyeong-Jin;Lee, Joun-Ho;Hegmann, Torsten;Jakli, Antal. And the article was included in Liquid Crystals in 2018.Synthetic Route of C6H5ClO2 The following contents are mentioned in the article:

We present studies on 21 multi-component mixtures consisting of bent-core liquid crystals to obtain room temperature switching between optically isotropic and birefringent states. Four of the mixtures show a significant enhancement over our previous results that were obtained either only at elevated temperatures, or did not show switching at room temperatures with appreciable contrast or speed. Although the switching of the new mixtures still requires high fields and shows only speeds at �00 ms, the results appear already useful for specific applications, such as transparent displays, that do not require video-rate switching and fast refresh rates of the content. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Synthetic Route of C6H5ClO2).

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).Synthetic Route of C6H5ClO2

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

Heterogeneously Catalyzed Pechmann Condensation Employing the Tailored Zn_0.925Ti_0.075O NPs: Synthesis of Coumarin was written by Jadhav, Nirajkumar H.;Sakate, Sachin S.;Rasal, Nishant K.;Shinde, Dnyaneshwar R.;Pawar, Ramdas A.. And the article was included in ACS Omega in 2019.Computed Properties of C6H5ClO2 The following contents are mentioned in the article:

A novel heterogeneous catalytic method was developed for the synthesis of coumarin and its derivatives using the Ti(IV)-doped ZnO matrix forming catalyst Zn_0.925Ti_0.075O having a high surface area and good Lewis acidity. The catalyst shows high activity toward a broad spectrum of the substituted phenols with β-ketoesters such as Et acetoacetate, Et butyryl acetate, Et benzoyl acetate, and so forth in good yields over short reaction times during the synthesis of coumarins. The methodol. was further extended for the synthesis of ayapin mols. The catalyst also shows recycle activity up to seven cycles with very good stability. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Computed Properties 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. 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.Computed Properties of C6H5ClO2

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

Iron-catalyzed arene C-H hydroxylation was written by Cheng, Lu;Wang, Huihui;Cai, Hengrui;Zhang, Jie;Gong, Xu;Han, Wei. And the article was included in Science (Washington, DC, United States) in 2021.Computed Properties of C6H5ClO2 The following contents are mentioned in the article:

Report of iron coordinated by a bioinspired l-cystine-derived ligand catalyzed undirected arene carbon-hydrogen hydroxylation with hydrogen peroxide as the terminal oxidant to afford aryl alcs. Ar-OH [Ar = Ph, N-(phenyl)acetamide, tert-butyl(phenyl)carbamate, etc.]. The reaction was distinguished by its broad substrate scope, excellent selectivity, good yields, and it showcased compatibility with oxidation-sensitive functional groups, such as alcs., polyphenols, aldehydes and even a boronic acid. This method was well suited for the synthesis of polyphenols through multiple carbon-hydrogen hydroxylations, as well as the late-stage functionalization of natural products and drug mols. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Computed Properties 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.Computed Properties of C6H5ClO2

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

Synthesis of substituted ureas possessing alkyl aromatic fragments via the reaction of 1-(3,3-diethoxypropyl)ureas with phenols was written by Smolobochkin, Andrey V.;Gazizov, Almir S.;Burilov, Alexander R.;Pudovik, Michail A.. And the article was included in Synthetic Communications in 2018.HPLC of Formula: 95-88-5 The following contents are mentioned in the article:

In this article, the approach to the substituted ureas based on the reaction of 1-(3,3-diethoxypropyl)ureas I [R¹ = R² = Me, i-Pr, Ph; R¹R² = (CH₂)₂O(CH₂)₂; R³ = R⁴ = OEt] with phenols was reported. Depending on the nature of the phenol and urea the reaction led either to diarylpropanes I [R³ = R⁴ = 5-Cl-2,4-di-HO-C₆H₂, 2,7-di-HO-1-naphthyl] and dibenzoxanthene derivatives or calixarenes. The proposed method benefited from mild reaction conditions, high product yields and operational simplicity. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5HPLC of Formula: 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. 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.HPLC of Formula: 95-88-5

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

Acyl Donors and Additives for the Biocatalytic Friedel-Crafts Acylation was written by Schmidt, Nina G.;Kroutil, Wolfgang. And the article was included in European Journal of Organic Chemistry in 2017.Recommanded Product: 4-Chlororesorcinol The following contents are mentioned in the article:

The Friedel-Crafts acylation is a broadly applied reaction that can be conducted using various types of catalyst. However, a biocatalytic alternative has only been reported recently. In this study, the scope of acetyl donors is described, showing that, in addition to vinyl acetate derivatives, Ph esters are also suitable donors. Furthermore, it was found that various amines enhance the reaction, whereby the effect do not seem to be correlated to the pH but to the structure of the donor. For instance, 1,4-diazabicyclo[2.2.2]octane (DABCO) turned out to be a viable alternative to imidazole; however the former performed best at pH 9.85, whereas the latter performed best at pH 8.3. 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