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N-[2-(acetylamino)-1,2-diphenylethyl]benzamide is a complex organic compound with the molecular formula C22H22N2O2. It is a derivative of benzamide, featuring a benzene ring attached to an amide group. The molecule contains a 1,2-diphenylethyl moiety, which is a three-carbon chain with two phenyl groups attached to the first and second carbons, respectively. The second carbon also bears an acetylamino group, which is an acetamide group attached to an amino group. This chemical structure endows the compound with potential pharmaceutical properties, as it may interact with biological targets through its amide and acetamide functionalities. The compound is synthesized for research purposes, particularly in the field of medicinal chemistry, to explore its effects on various biological systems and its potential as a therapeutic agent.

6944-06-5

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6944-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6944-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6944-06:
(6*6)+(5*9)+(4*4)+(3*4)+(2*0)+(1*6)=115
115 % 10 = 5
So 6944-06-5 is a valid CAS Registry Number.

6944-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-acetamido-1,2-diphenylethyl)benzamide

1.2 Other means of identification

Product number -
Other names n-[2-(acetylamino)-1,2-diphenylethyl]benzamide

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:6944-06-5 SDS

6944-06-5Relevant academic research and scientific papers

Nitroacetamidation of Styrenes

Bloom, A. Jon,Fleischmann, Martin,Mellor, John M.

, p. 2357 - 2362 (2007/10/02)

Reaction of styrenes with nitronium tetrafluoroborate in acetonitrile affords good yields of products of nitroacetamidation.In all cases addition is highly regeoselective to give Markownikoff products.With trans-β-methylstyrene, conversion of the initial

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