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N,N-dibenzylbut-2-enediamide is a chemical compound with the molecular formula C20H22N2O2. It is a derivative of but-2-enediamide, featuring two benzyl groups attached to the nitrogen atoms. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. Its structure provides a rigid framework that can be utilized in the design of molecules with specific properties, such as improved stability or bioavailability. The compound's unique arrangement of atoms and functional groups also makes it a subject of interest in organic chemistry research, where it can be used to study the effects of steric hindrance and electronic interactions on chemical reactivity and physical properties.

5240-54-0

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5240-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5240-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,4 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5240-54:
(6*5)+(5*2)+(4*4)+(3*0)+(2*5)+(1*4)=70
70 % 10 = 0
So 5240-54-0 is a valid CAS Registry Number.

5240-54-0SDS

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'-dibenzylbut-2-enediamide

1.2 Other means of identification

Product number -
Other names N,N-DIBENZYLBUT-2-ENEDIAMIDE

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:5240-54-0 SDS

5240-54-0Downstream Products

5240-54-0Relevant academic research and scientific papers

Efficient synthesis of fumaric amides through cross-metathesis of acrylic amides with the NHC Grubbs ruthenium catalyst

Streuff, Jan,Mu?iz, Kilian

, p. 5973 - 5978 (2007/10/03)

Application of the second generation Grubbs metathesis catalyst for the homo-cross-metathesis of acroyl amides from chiral amines is reported. This efficient and high-yielding reaction provides a side-product free synthesis of fumaric acid diamides which

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