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4664-73-7

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4664-73-7 Usage

Structure

Cyclohexanecarboxamide derivative with a chlorine atom and a phenyl group attached to the nitrogen atom

Physical state

White crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Applications

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Functional groups

Amide functional group

Reactivity

Suitable for use as a coupling agent in organic reactions

Check Digit Verification of cas no

The CAS Registry Mumber 4664-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4664-73:
(6*4)+(5*6)+(4*6)+(3*4)+(2*7)+(1*3)=107
107 % 10 = 7
So 4664-73-7 is a valid CAS Registry Number.

4664-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-N-phenylcyclohexane-1-carboxamide

1.2 Other means of identification

Product number -
Other names 1-Chlor-cyclohexan-1-carbonsaeure-anilid

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:4664-73-7 SDS

4664-73-7Downstream Products

4664-73-7Relevant articles and documents

Dichloromethane as a chlorination reagent for α-bromocarbonyl compounds in the presence of a copper catalyst

Takeuchi, Kentaro,Ishida, Syo,Nishikata, Takashi

supporting information, p. 644 - 646 (2017/08/30)

We found that dichloromethane is a powerful chlorinating reagent for the congested 3° and 2° Csp3Br bond of α-bromocarbonyl amides, esters, and ketones. In the presence of an appropriate copper complex as a catalyst, the desired chlorination occurred within an hour. Control experiments revealed that in situ-generated CuCl2 is a key chlorinating agent that reacts with the 3° or 2° alkyl radicals generated by the reaction between an α-bromocarbonyl compound and a Cu(I) salt.

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