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N-(2-oxo-1,2-diphenylethyl)-N-phenylacetamide is a complex organic compound with the molecular formula C20H17NO2. It is a derivative of acetamide, featuring a phenyl group attached to the nitrogen atom and a 2-oxo-1,2-diphenylethyl group connected to the nitrogen as well. N-(2-oxo-1,2-diphenylethyl)-N-phenylacetamide is characterized by its two phenyl rings and a central carbonyl group, which contributes to its structural stability. It is a white crystalline solid and is often used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The compound's properties, such as its melting point and solubility, can be influenced by the presence of the phenyl groups and the carbonyl functionality, making it a versatile building block in organic chemistry.

5326-56-7

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5326-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5326-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5326-56:
(6*5)+(5*3)+(4*2)+(3*6)+(2*5)+(1*6)=87
87 % 10 = 7
So 5326-56-7 is a valid CAS Registry Number.

5326-56-7SDS

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 N-(2-oxo-1,2-diphenylethyl)-N-phenylacetamide

1.2 Other means of identification

Product number -
Other names N-Desyl-acetanilid

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:5326-56-7 SDS

5326-56-7Relevant academic research and scientific papers

THE SELECTIVE REDUCTIVE ACYLATION OF α-KETO IMINES

Alper, Howard,Amaratunga, Shiyamaline

, p. 3811 - 3812 (2007/10/02)

Reaction of α-keto imines with the in situ generated acetylcobalt tetracarbonyl occurs only at the carbon-nitrogen double bond to give β-keto amides.An unexpected by-product was formed in several instances.

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