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39918-94-0

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39918-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39918-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,1 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39918-94:
(7*3)+(6*9)+(5*9)+(4*1)+(3*8)+(2*9)+(1*4)=170
170 % 10 = 0
So 39918-94-0 is a valid CAS Registry Number.

39918-94-0SDS

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 S-[(4-chlorophenyl)methyl] N-ethylcarbamothioate

1.2 Other means of identification

Product number -
Other names Carbamothioic acid,ethyl-,S-[(4-chlorophenyl)methyl] 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:39918-94-0 SDS

39918-94-0Upstream product

39918-94-0Downstream Products

39918-94-0Relevant articles and documents

Thiobencarb degradation by TiO2 photocatalysis: Parameter and reaction pathway investigations

Lai, Hsiao-Fang,Chen, Chiing-Chang,Wu, Ren-Jang,Lu, Chung-Shin

, p. 87 - 97 (2012)

The present study deals with the photocatalytic degradation of the thiocarbamate herbicide, thiobencarb (TBC), in the presence of TiO2 particles and UV-A (λ = 365 nm) radiation. Results show rapid and complete oxidation of TBC after 90 min, and slightly over 70% of TBC was mineralized after 32-h treatment. Factors such as solution pH, TiO2 dosage, and the presence of anions are found to influence the degradation rate. The establishment of the reaction pathway is made possible by a thorough analysis of the reaction mixture identifying the main intermediate products generated. Results suggest that possible transformation pathways may include hydroxylation, dealkylation and C-S bond cleavage processes. The possible degradation pathways are proposed and discussed on the basis of the evidence of oxidative intermediate formation.

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