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"o-Phenyl (2-chlorophenyl)carbamothioate" is a chemical compound with the molecular formula C13H10ClNOS. It is an organosulfur compound that belongs to the class of carbamothioates, which are derivatives of carbamic acid. This specific compound features an o-phenyl group (a phenyl group attached to the second carbon of another phenyl ring) and a 2-chlorophenyl group (a phenyl ring with a chlorine atom at the second position), both connected to a central carbamothioate structure. It is known for its potential applications in the synthesis of various organic compounds and as an intermediate in the production of pesticides and pharmaceuticals. Due to its chemical structure, it may exhibit specific reactivity and properties that are relevant to its use in these industries.

785-50-2

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785-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 785-50-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 785-50:
(5*7)+(4*8)+(3*5)+(2*5)+(1*0)=92
92 % 10 = 2
So 785-50-2 is a valid CAS Registry Number.

785-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name o-phenyl (2-chlorophenyl)carbamothioate

1.2 Other means of identification

Product number -
Other names N-[2-Chlor-phenyl]-O-phenyl-thionurethan

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:785-50-2 SDS

785-50-2Downstream Products

785-50-2Relevant academic research and scientific papers

Synthesis of isothiocyanates by reaction of amines with phenyl chlorothionoformate via one-pot or two-step process

Li, Zheng-Yi,Ma, Hong-Zhao,Han, Chen,Xi, Hai-Tao,Meng, Qi,Chen, Xin,Sun, Xiao-Qiang

, p. 1667 - 1674 (2013)

A facile and efficient synthesis of isothiocyanates from amines is described. This method involves the reaction of amines with phenyl chlorothionoformate in the presence of solid sodium hydroxide by either a one-pot process or a two-step approach. The one-pot process is useful for preparing alkyl and electron-rich aryl isothiocyanates, whereas the two-step approach is more versatile, working very well not only for alkyl and electron-rich aryl isothiocyanates, but also for highly electron-deficient aryl and heterocyclic isothiocyanates. Georg Thieme Verlag Stuttgart, New York.

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