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1-Imidazolidinecarboxylic acid, 3-methyl-2-oxo-, 4-nitrophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87768-63-6

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87768-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87768-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87768-63:
(7*8)+(6*7)+(5*7)+(4*6)+(3*8)+(2*6)+(1*3)=196
196 % 10 = 6
So 87768-63-6 is a valid CAS Registry Number.

87768-63-6SDS

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 (4-nitrophenyl) 3-methyl-2-oxoimidazolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1N-paranitrophenoxycarbonyl-3N-methyl-2-imidazolidinone

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:87768-63-6 SDS

87768-63-6Relevant academic research and scientific papers

HYDROLYSE BASIQUE COMPAREE D'ESTERS ALLOPHANIQUES ET PHOSPHORIQUES EN MILIEU MIXTE ACETONITRILE/EAU FAIBLEMENT AQUEUX; MISE EN EVIDENCE D'UNE ENTITE CATALIQUE, INTERMEDIARE DE LA REACTION ENTRE BASE ET SOLVANT

Monnier, Par E.,Botella, J. M.,Murillo, A.,Klaebe, A.,Perie, J.

, p. 1315 - 1332 (1986)

Kinetic study of base catalysed hydrolysis in acetonitrile-water mixtures of allophanic esters (models of carboxybiotine) and phosphoric esters shows in the range of low water content (less than 1 molar) an enhancement in rate (103) with a maximum at 0.1-0.3 molar in water.This rate enhancement is ascribed to ground state desolvation and the maximum is interpreted by a change in the rate determining step: leaving group departure in the tetrahedral intermediate is indeed the slow step for the reactions in acetonitrile/water mixture less than 0.1 molar in water.For charged phosphoric esters the rate enhancement from an aqueous medium (pH=10) to organic is larger since as high as 106.On the other hand, in such a medium, an additional catalytic effect is observed; it is shown that it is due to the formation of a reactive species which results from reaction of the base on acetamide when accumulated in the medium from base catalysed hydrolysis of the solvent.

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