Cominetti, Marco M. D. et al. published their research in Organic & Biomolecular Chemistry in 2016 | 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Safety of 4-Chlororesorcinol

Open-resorcinarenes, a new family of multivalent scaffolds was written by Cominetti, Marco M. D.;Hughes, David L.;Matthews, Susan E.. And the article was included in Organic & Biomolecular Chemistry in 2016.Safety of 4-Chlororesorcinol The following contents are mentioned in the article:

A new family of multivalent ligand platforms, the open-resorcinarenes, was prepared in a straightforward two-step reaction. Modification of the core gave a range of topol. diverse scaffolds; functionalisation confirmed the versatility of this approach, as shown through the formation of an octacalixarene array. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Safety of 4-Chlororesorcinol).

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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Safety of 4-Chlororesorcinol

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

Smolobochkin, Andrey V. et al. published their research in ChemistrySelect in 2019 | 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. 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.Name: 4-Chlororesorcinol

Reactions of 1-(3,3-Diethoxypropyl)urea with Phenols: Synthesis of 1,6-Disubstituted Tetrahydropyrimidine-2(1H)-ones was written by Smolobochkin, Andrey V.;Gazizov, Almir S.;Voronina, Julia K.;Strelnik, Anna G.;Rizbayeva, Tanzilya S.;Burilov, Alexander R.;Pudovik, Michail A.. And the article was included in ChemistrySelect in 2019.Name: 4-Chlororesorcinol The following contents are mentioned in the article:

A new approach to the synthesis of 1,6-disubstituted tetrahydropyrimidine-2(1H)-ones via the acid-catalyzed reaction of (3,3-diethoxypropyl)urea with various phenols was proposed. The proposed approach allowed to obtain target compounds in one-pot manner and without the use of expensive reagents and catalysts. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Name: 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 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.Name: 4-Chlororesorcinol

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

Chavhan, JV. et al. published their research in International Journal of Pharmaceutical, Chemical and Biological Sciences 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.Recommanded Product: 4-Chlororesorcinol

Synthesis, structural elucidation, and antibacterial evaluation of some flavones derived from coumarin was written by Chavhan, JV.;Patil, SS.. And the article was included in International Journal of Pharmaceutical, Chemical and Biological Sciences in 2018.Recommanded Product: 4-Chlororesorcinol The following contents are mentioned in the article:

In the present study, substituted coumarin-based flavones I (R = OH, Cl) were synthesized via chalcones. The reactions were easily conducted under mild conditions and gave I in good yields. The synthesized compounds were evaluated against four strains of bacterial culture. 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. 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.Recommanded Product: 4-Chlororesorcinol

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

Smolobochkin, A. V. et al. published their research in Russian Journal of Organic Chemistry 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.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.Electric Literature of C6H5ClO2

Synthesis of 1-(arylsulfonyl)pyrrolidines from aryl alcohols and 1-[(4-chlorophenyl)sulfonyl]-2-ethoxypyrrolidine was written by Smolobochkin, A. V.;Anikina, E. A.;Gazizov, A. S.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of Organic Chemistry in 2017.Electric Literature of C6H5ClO2 The following contents are mentioned in the article:

Acid-catalyzed reaction of 1-[(4-chlorophenyl)sulfonyl]-2-ethoxypyrrolidine with aryl alcs. led to the formation of new 1-(arylsulfonyl)pyrrolidines. The reaction proceeded under mild conditions and might be used as a convenient method for the synthesis of pyrrolidine-1-sulfonylarene derivatives containing a phenol fragment in the position 2. 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.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.Electric Literature of C6H5ClO2

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

Gazizov, Almir S. et al. published their research in Synlett in 2018 | CAS: 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. 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

Acid-Mediated C-N Bond Cleavage in 1-Sulfonylpyrrolidines: An Efficient Route towards Dibenzoxanthenes, Diarylmethanes, and Resorcinarenes was written by Gazizov, Almir S.;Smolobochkin, Andrey V.;Anikina, Ekaterina A.;Strelnik, Anna G.;Burilov, Alexander R.;Pudovik, Michail A.. And the article was included in Synlett in 2018.Synthetic Route of C6H5ClO2 The following contents are mentioned in the article:

The rare example of pyrrolidine C-N bond cleavage in 1-sulfonylpyrrolidines in acidic media in the presence of phenols is reported. The reaction proceeds under mild conditions and provides a convenient route to otherwise hardly accessible and previously unknown dibenzoxanthenes, diarylbutanes, and resorcinarenes having a sulfonylamide moiety. 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 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. 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

Cui, Yu-Ang et al. published their research in Asian Journal of Organic Chemistry in 2022 | 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.Application of 95-88-5

Microwave-Assisted Synthesis of d/l-Agrimonolide was written by Cui, Yu-Ang;Zhang, Guang-Yu;Li, Yun-Zhi;Li, Wei;Tanabe, Genzoh;Osamu, Muraoka;Xie, Wei-Jia. And the article was included in Asian Journal of Organic Chemistry in 2022.Application of 95-88-5 The following contents are mentioned in the article:

In this study, authors reported an improved approach for the synthesis of d/l Agrimonolide from 4-chlororesorcinol. It was found that a microwave assisted intramol. esterification is an effective way to construct the 3,4-dihydroisocoumarin core structure. The target d/l Agrimonolide is obtained in 7 steps with the overall yields of 20.7%. 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. 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.Application of 95-88-5

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

Zhao, Yuan et al. published their research in Bioorganic & Medicinal Chemistry Letters 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.Safety of 4-Chlororesorcinol

Facile synthesis of acacetin and its derivatives was written by Zhao, Yuan;Cai, Li;Sui, Qiang;Lin, Feng;Jiang, Wen;Chen, Jianli;Lu, Weigeng;Gao, Qi. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2016.Safety of 4-Chlororesorcinol The following contents are mentioned in the article:

Acacetin, an O-methylated bioflavonoid isolated from the traditional Chinese medicine Xuelianhua (Saussurea tridactyla), is a promising orally effective atrium-selective antiarrhythmic agent for the treatment of atrial fibrillation (AF). Here we describe an efficient two-component method for the synthesis of acacetin and its derivatives This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Safety of 4-Chlororesorcinol).

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.Safety of 4-Chlororesorcinol

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

Uchida, Keisuke et al. published their research in Synthesis in 2016 | 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. 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.Application of 95-88-5

Controlled Generation of 3-Triflyloxyarynes was written by Uchida, Keisuke;Yoshida, Suguru;Hosoya, Takamitsu. And the article was included in Synthesis in 2016.Application of 95-88-5 The following contents are mentioned in the article:

3-Triflyloxyarynes such as 3-triflyloxybenzyne, including those bearing a transformable group, were prepared by iodine-magnesium exchange reactions of 1,3-bis(triflyloxy)-2-iodoarenes such as I using conditions that efficiently suppressed the competing thia-Fries rearrangement. The method enabled the facile synthesis of a wide range of multisubstituted arenes such as II. 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. 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. 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.Application of 95-88-5

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

Smolobochkin, Andrey V. et al. published their research in Chemistry of Heterocyclic Compounds in 2017 | CAS: 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. 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).Name: 4-Chlororesorcinol

Acid-catalyzed reaction of phenols with N-(4,4-diethoxybutyl)sulfonamides – a new method for the synthesis of 2-aryl-1-sulfonylpyrrolidines was written by Smolobochkin, Andrey V.;Gazizov, Almir S.;Anikina, Ekaterina A.;Burilov, Alexander R.;Pudovik, Michael A.. And the article was included in Chemistry of Heterocyclic Compounds in 2017.Name: 4-Chlororesorcinol The following contents are mentioned in the article:

A new method for the synthesis of 2-aryl-1-sulfonylpyrrolidines I (R = Me, Et, Ph, p-tolyl; R1 = 5-chloro-2,4-dihydroxyphenyl, 2-hydroxynaphthalen-1-yl, 2,7-dihydroxynaphthalen-1-yl) on the basis of reactions between various phenols ArH and N-(4,4-diethoxybutyl)sulfonamides RS(O)2NH(CH2)3CH(OEt)2 in the presence of trifluoroacetic acid has been developed. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Name: 4-Chlororesorcinol).

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. 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).Name: 4-Chlororesorcinol

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

Haeussler, Daniela et al. published their research in Synthesis in 2016 | 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Computed Properties of C6H5ClO2

Fluorescently labeled amino acids as building blocks for bioactive molecules was written by Haeussler, Daniela;Guetschow, Michael. And the article was included in Synthesis in 2016.Computed Properties of C6H5ClO2 The following contents are mentioned in the article:

A series of twelve fluorescently labeled amino acids were designed by assembling different coumarin, fluorescein, or nitrobenzofurazan fluorophores with N-protected lysine or 2-aminopropionic acid. The synthesized amino acids were evaluated with regard to their spectroscopic properties. The easy introduction of the amino acids into peptides and peptidomimetics was exemplarily shown for one coumarin-labeled amino acid. 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. 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. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Computed Properties of C6H5ClO2

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