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Carbamothioic acid, (4-nitrophenyl)-, S-phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77499-95-7

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77499-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77499-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77499-95:
(7*7)+(6*7)+(5*4)+(4*9)+(3*9)+(2*9)+(1*5)=197
197 % 10 = 7
So 77499-95-7 is a valid CAS Registry Number.

77499-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitro-phenyl)-thiocarbamic acid S-phenyl ester

1.2 Other means of identification

Product number -
Other names (4-Nitro-phenyl)-thiocarbamidsaeure-S-phenylester

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:77499-95-7 SDS

77499-95-7Relevant academic research and scientific papers

HYDROLYSIS KINETICS AND MECHANISM OF DIARYLTHIOCARBAMATES IN 20percent AQUEOUS DIOXANE MEDIUM

Mindl, Jaromir,Balcarek, Pavel,Silar, Lubomir,Vecera, Miroslav

, p. 3130 - 3139 (2007/10/02)

Substituted S-aryl and O-aryl N-arylthiocarbamates have been synthetized.Kinetic studies of hydrolysis of these compounds in 20percent aqueous dioxane prove the ElcB mechanism.The found Hammett reaction constants, activation entropy values, Broensted coefficients, and comparison of reactivity with N-methyl analogues have been discussed as criteria of the mentioned mechanism.Hydrolysis results of thiocarbamates and carbamates in the same medium are compared.

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