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2-Chloro-4-cyclohexylphenol is an organic compound with the chemical formula C12H15ClO. It is a derivative of phenol, featuring a cyclohexyl group attached to the para position (4th position) and a chlorine atom at the ortho position (2nd position). This white crystalline solid is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its potential applications and chemical properties, 2-chloro-4-cyclohexylphenol is of interest in the fields of organic chemistry and chemical engineering.

3964-61-2

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3964-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3964-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,6 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3964-61:
(6*3)+(5*9)+(4*6)+(3*4)+(2*6)+(1*1)=112
112 % 10 = 2
So 3964-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H15ClO/c13-11-8-10(6-7-12(11)14)9-4-2-1-3-5-9/h6-9,14H,1-5H2

3964-61-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4-cyclohexylphenol

1.2 Other means of identification

Product number -
Other names Phenol, 2-chloro-4-cyclohexyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3964-61-2 SDS

3964-61-2Relevant academic research and scientific papers

(2R)-2-Methylchromane-2-carboxylic acids: Discovery of selective PPARα agonists as hypolipidemic agents

Koyama, Hiroo,Boueres, Julia K.,Miller, Daniel J.,Berger, Joel P.,MacNaul, Karen L.,Wang, Pei-Ran,Ippolito, Marc C.,Wright, Samuel D.,Agrawal, Arun K.,Moller, David E.,Sahoo, Soumya P.

, p. 3347 - 3351 (2007/10/03)

A SAR study was conducted on chromane-2-carboxylic acid toward selective PPARα agonisim. As a result, highly potent, and selective PPARα agonists were discovered. The optimized compound 43 exhibited robust lowering of total cholesterol levels in hamster and dog animal models.

ALKYLATION OF 2- AND 4-CHLOROPHENOLS BY ALKYL HALIDES IN THE PRESENCE OF SMALL AMOUNTS OF CATALYSTS

Alieva, M. K.,Akhmedov, K. N.

, p. 1850 - 1853 (2007/10/02)

The alkylation of 2-chlorophenol by benzyl chloride, chlorocyclohexane, chlorocyclopentane, sec-butyl bromide, and 1- and 2-bromopentanes in the presence of 1.06.10-3 - 1.06.10-2 mole of catalyst (a Lewis acid) was investigated.Competing alkylations of chlorophenols and phenol with benzyl chloride, realized under identical conditions, showed that the reactivity of the substrate decreases in the order: phenol > 3-chlorophenol > 4-chlorophenol >= 2-chlorophenol.The ratio of the 6- and 4-isomers of benzyl-2-chlorophenols is not affected by the nature of the anion in the catalyst.During the alkylation of 4-chlorophenol with butyl bromide and bromopentane the main product is sec-alkyl-4-chlorophenol (yield 86-90percent), and 4-9percent of the alkyl-4-chlorophenol is formed.

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