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27163-66-2

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27163-66-2 Usage

Physical state

Colorless to pale yellow liquid

Odor

Sweet

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Intermediate in the synthesis of pharmaceuticals
b. Intermediate in the synthesis of agrochemicals
c. Building block for the production of other organic compounds
d. Research chemical

Hazard classification

Classified as a hazardous substance

Precautions

a. Care should be taken when handling to avoid exposure
b. Proper storage to prevent environmental contamination

Check Digit Verification of cas no

The CAS Registry Mumber 27163-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27163-66:
(7*2)+(6*7)+(5*1)+(4*6)+(3*3)+(2*6)+(1*6)=112
112 % 10 = 2
So 27163-66-2 is a valid CAS Registry Number.

27163-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-cyclohexylbenzene

1.2 Other means of identification

Product number -
Other names -

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:27163-66-2 SDS

27163-66-2Downstream Products

27163-66-2Relevant articles and documents

Ruthenium-catalyzed para-selective oxidative cross-coupling of arenes and cycloalkanes

Guo, Xiangyu,Li, Chao-Jun

supporting information; experimental part, p. 4977 - 4979 (2011/11/12)

A novel, direct para-selective oxidative cross-coupling of benzene derivatives with cycloalkanes catalyzed by ruthenium was developed. A wide range of arenes bearing electron-withdrawing substituents was functionalized directly with simple cycloalkanes with high para-selectivity; arenes with electron-donating groups were mainly para-functionalized. Benzoic acid can be used directly.

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