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185390-53-8

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185390-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185390-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 185390-53:
(8*1)+(7*8)+(6*5)+(5*3)+(4*9)+(3*0)+(2*5)+(1*3)=158
158 % 10 = 8
So 185390-53-8 is a valid CAS Registry Number.

185390-53-8SDS

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 (4-cyanophenyl) 2-phenoxyacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,phenoxy-,4-cyanophenyl ester

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:185390-53-8 SDS

185390-53-8Relevant articles and documents

Kinetics of Aminolysis of Phenyl Phenoxyacetates with Benzylamines in Acetonitrile

Koh, Han Joong,Kim, Tae Hyoung,Lee, Bon-Su,Lee, Ikchoon

, p. 2741 - 2751 (2007/10/03)

Kinetic studies are carried out on the reactions of benzylamines with phenyl phenoxyacetates in acetonitrile.Based on (i) the large magnitude of various selectivity parameters, ρx, ρz and ρxz, (ii) the normal kinetic isotope effects (kH/kD > 1.0) involving deuterated benzylamine nucleophiles and (iii) the low entalpies and entropies of activation, it was cocncluded that the reactions proceed by a stepwise mechanism with rate-limiting breakdown of the tetrahedral zwitterionic intermadiate.There are, however, two pathways in the rate-limiting breakdown step of the intermediate, the uncatalysed and base-catalysed.The latter path is characterized by the larger ρxz and kH/kD values, and lower activation parameters than those the uncatalyzed path.

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