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2-Hydroxyethyl phenylcarbamate, also known as phenolcarbamate or phenol carbamate, is an organic compound with the chemical formula C8H9NO3. It is a colorless, crystalline solid that is soluble in water and has a molecular weight of 167.16 g/mol. 2-hydroxyethyl phenylcarbamate is formed by the reaction of phenol with chloroethyl carbonate, and it is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. 2-Hydroxyethyl phenylcarbamate is also known for its potential use as a chemical warfare agent, due to its ability to inhibit the enzyme acetylcholinesterase, which is crucial for the proper functioning of the nervous system. However, it is important to note that the use of such chemicals for warfare is prohibited under international law.

709-93-3

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709-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 709-93-3 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 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 709-93:
(5*7)+(4*0)+(3*9)+(2*9)+(1*3)=83
83 % 10 = 3
So 709-93-3 is a valid CAS Registry Number.

709-93-3SDS

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 2-hydroxyethyl N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names MONO(PHENYLCARBAMATE)-1,2-ETHANEDIOL

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:709-93-3 SDS

709-93-3Relevant academic research and scientific papers

CO2 activation and fixation: highly efficient syntheses of hydroxy carbamates over Au/Fe2O3

Shang, Jianpeng,Guo, Xiaoguang,Li, Zuopeng,Deng, Youquan

, p. 3082 - 3088 (2016/06/06)

This paper reports an effective route for the syntheses of hydroxy carbamates from the reaction of CO2, epoxides and amines catalyzed by a Au/Fe2O3 catalyst. Under the optimized reaction conditions, various hydroxy carbamates were successfully synthesized with 92-98% isolated yields. The catalyst could be reused for several runs without deactivation. A plausible reaction mechanism was proposed by which the hydroxy carbamate was formed through an ammonium carbamate intermediate and the catalyst mainly promoted further nucleophilic addition between the epoxide and ammonium carbamate.

The influence of the structure of alcohols on the rate of N,N'-diphenylurea alcoholysis

Mantrov,Chimyashkin

, p. 688 - 691 (2007/10/03)

The kinetics and mechanism of the reaction between symmetrical diphenylurea and various alcohols in the absence of inert solvents were studied. The activation parameters of alcoholysis were determined. A correlation equation that described the influence of the nature of the alcohol on the rate of the reaction was obtained. Copyright

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