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1H-Pyrrole-3-carboxylic acid, 1-benzoyl-2,5-dihydro-2-phenyl, methyl ester is a complex organic compound with the molecular formula C18H15NO3. It is a derivative of pyrrole, a heterocyclic aromatic organic compound containing four carbon atoms and one nitrogen atom in a five-membered ring. The compound features a benzoyl group attached to the nitrogen atom, a phenyl group at the 2-position, and a methyl ester group at the 3-position. This molecule is characterized by its unique structure and properties, which may have potential applications in various fields such as pharmaceuticals, materials science, and chemical research.

79962-70-2

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79962-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79962-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,6 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79962-70:
(7*7)+(6*9)+(5*9)+(4*6)+(3*2)+(2*7)+(1*0)=192
192 % 10 = 2
So 79962-70-2 is a valid CAS Registry Number.

79962-70-2SDS

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 1-Benzoyl-2-phenyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid methyl ester

1.2 Other means of identification

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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

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More Details:79962-70-2 SDS

79962-70-2Relevant academic research and scientific papers

NEW 1,3-DIPOLAR CYCLOADDITION LEADING TO 2,5-DIHYDROPYRROLE AND PYRROLIDINE DERIVATIVES

Achiwa, Kazuo,Sekiya, Minoru

, p. 1213 - 1216 (1981)

A novel 1,3-cycloaddition of intermediaries derived from N-(benzylidene)trimethylsilylmethylamine and acyl chlorides to conjugated olefins and acetylenes gave pyrrolidine and 2,5-dihydropyrrole derivatives, respectively.

1,3-Dipolar Cycloaddition Leading to N-Acylated Pyrrolidines and 2,5-Dihydropyrroles

Achiwa, Kazuo,Motoyama, Tadashi,Sekiya, Minoru

, p. 3939 - 3945 (2007/10/02)

Dipolar cycloaddition of an intermediary N-acyltrimethylsilylmethyliminium salt formed from N-(benzylidene)trimethylsilylmethylamine and acyl chloride to conjugated alkenes or alkines gave N-acylpyrrolidines or N-acyl-2,5-dihydropyrroles, respectively.The

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