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N,N-dibenzyl-2-chlorobenzamide is a chemical compound with the molecular formula C20H18ClNO. It is a white crystalline solid that is soluble in organic solvents such as ethanol, acetone, and dichloromethane. N,N-dibenzyl-2-chlorobenzamide is primarily used as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals, particularly in the synthesis of benzamide derivatives. The presence of the chloro group in the molecule allows for further functionalization and substitution reactions, making it a versatile building block in organic chemistry. N,N-dibenzyl-2-chlorobenzamide is also known for its potential applications in the development of new drugs targeting various therapeutic areas, such as central nervous system disorders and cancer.

7465-70-5

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7465-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7465-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7465-70:
(6*7)+(5*4)+(4*6)+(3*5)+(2*7)+(1*0)=115
115 % 10 = 5
So 7465-70-5 is a valid CAS Registry Number.

7465-70-5SDS

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 N,N-dibenzyl-2-chlorobenzamide

1.2 Other means of identification

Product number -
Other names 2-Chlor-N,N-dibenzylbenzamid

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:7465-70-5 SDS

7465-70-5Relevant academic research and scientific papers

POTENTIAL CENTRAL NERVOUS SYSTEM ACTIVE AGENTS. 3. SYNTHESIS OF SOME SUBSTITUTED BENZAMIDES AND PHENYLACETAMIDES.

Agwada

, p. 231 - 235 (2007/10/02)

The preparation and special properties (IR, **1H NMR) are given for 45 benzamides and 10 phenylacetamides substituted on nitrogen with allyl, benzhydryl, benzyl, or cyclopropyl groups, and variously substituted on the acyl part with halo, methoxyl, methyl, or nitro groups. The benzamide derivatives were synthesized by the Schotten-Baumann method, and the phenylacetamide derivatives were prepared by heating the appropriate N-benzhydrylammonium salt in o-xylene. Thirty-one of the compounds are new.

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