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Pyrrolidine, 1-[[(phenylmethylene)amino]acetyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113273-60-2

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113273-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113273-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113273-60:
(8*1)+(7*1)+(6*3)+(5*2)+(4*7)+(3*3)+(2*6)+(1*0)=92
92 % 10 = 2
So 113273-60-2 is a valid CAS Registry Number.

113273-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzylideneamino)-1-pyrrolidin-1-ylethanone

1.2 Other means of identification

Product number -
Other names Pyrrolidine,1-[[(phenylmethylene)amino]acetyl]

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:113273-60-2 SDS

113273-60-2Relevant academic research and scientific papers

Lithium Bromide/Triethylamine Induced Cycloaddition of N-Alkylidene 2-Amino Esters and Amides to Electron-Deficient Olefins with High Regio- and Stereoselectivity

Tsuge, Otohiko,Kanemasa, Shuji,Yoshioka, Manabu

, p. 1384 - 1391 (2007/10/02)

The imines of 2-amino esters and amides derived from glycine, alanine, and valine are deprotonated by the action of a lithium halide and triethylamine (or DBU).The resulting anionic intermediates undergo highly regio- and stereoselective cycloadditions with a variety of olefins activated by carbonyl-type substituents to produce stereochemically defined derivatives of proline esters or amides.The scope and limitations of this novel cycloaddition are discussed.

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