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Carbamothioic acid, cyclohexyl-, O-ethyl ester is a chemical compound with the molecular formula C9H17NOS2. It is an organosulfur compound that belongs to the class of carbamothioates, which are derivatives of carbamic acid. This specific compound features a cyclohexyl group attached to the carbamothioic acid backbone, with an ethyl ester group at the oxygen atom. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. Carbamothioic acid, cyclohexyl-, O-ethyl ester is primarily used as an intermediate in the synthesis of various agrochemicals, particularly in the production of pesticides and herbicides. Due to its potential applications in agriculture, it is essential to handle Carbamothioic acid, cyclohexyl-, O-ethyl ester with care, as it may have toxic effects on non-target organisms and the environment.

705-75-9

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705-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705-75-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 705-75:
(5*7)+(4*0)+(3*5)+(2*7)+(1*5)=69
69 % 10 = 9
So 705-75-9 is a valid CAS Registry Number.

705-75-9SDS

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-hydroxyethylvinylnitrosamine

1.2 Other means of identification

Product number -
Other names -

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:705-75-9 SDS

705-75-9Relevant academic research and scientific papers

Syntheses of N-alkyl, A,N-dialkyl, and N-(4-substituted phenyl) O-ethyl thioncarbamates: A kinetic study

Milosavljevic, Milutin M.,Marinkovic, Aleksandar D.,Veljkovic, Vlada B.,Milenkovic, Dragan D.

experimental part, p. 43 - 49 (2012/07/13)

The kinetics of the syntheses of N-alkyl, N,N-dialkyl, and N-(4-substituted phenyl) O-ethyl thioncarbamates from sodium ethyl xanthogenacetate, ten alkylamines, and eight substituted anilines were studied at 25, 30, 35, and 40 °C. The reactions were found to follow second-order kinetics. The kinetic (Arrhenius) parameters, such as the activation energy and the frequency factor, as well as the Eyring parameters, such as the standard entropy, the standard Gibbs energy, and the standard enthalpy of activation, were calculated from the second-order rate constants. The mechanism of the reaction was postulated based on the kinetic studies presented and the optimization of the reaction mechanism using the MOPAC PM6 semi-empirical method.

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