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2-chloro-N-(3-nitrophenyl)-3-phenylpropanamide is a chemical compound with the molecular formula C15H12ClN2O3. It is an organic compound that belongs to the class of amides, specifically a substituted propanamide. 2-chloro-N-(3-nitrophenyl)-3-phenylpropanamide is characterized by the presence of a chloro group at the 2-position, a nitro group at the 3-position of the phenyl ring, and a phenyl group at the 3-position of the propanamide backbone. It is a yellow crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure and potential applications, it is important in the field of organic chemistry and drug development.

6632-27-5

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6632-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6632-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6632-27:
(6*6)+(5*6)+(4*3)+(3*2)+(2*2)+(1*7)=95
95 % 10 = 5
So 6632-27-5 is a valid CAS Registry Number.

6632-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-(3-nitrophenyl)-3-phenylpropanamide

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

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More Details:6632-27-5 SDS

6632-27-5Downstream Products

6632-27-5Relevant academic research and scientific papers

Synthesis and anti-parasitic activity of C-benzylated (N-arylcarbamoyl)alkylphosphonate esters

Adeyemi, Christiana M.,Isaacs, Michelle,Mnkandhla, Dumisani,Klein, Rosalyn,Hoppe, Heinrich C.,Krause, Rui W.M.,Lobb, Kevin A.,Kaye, Perry T.

, p. 1661 - 1667 (2017/03/08)

Unexpected substituent-dependent regioselectivty challenges in the synthesis of C-benzylated (N-arylcarbamoyl)phosphonate esters have been resolved. The C-benzylated N-furfurylcarbamoyl derivative showed low micromolar PfLDH inhibition, while one of the C-benzylated N-arylcarbamoyl analogues was active against Nagana Trypanosoma brucei parasites which are responsible for African trypanosomiasis in cattle.

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