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N-Allyldithiocarbamic acid phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62118-13-2

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62118-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62118-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,1 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62118-13:
(7*6)+(6*2)+(5*1)+(4*1)+(3*8)+(2*1)+(1*3)=92
92 % 10 = 2
So 62118-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NS2/c1-2-8-11-10(12)13-9-6-4-3-5-7-9/h2-7H,1,8H2,(H,11,12)

62118-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl N-prop-2-enylcarbamodithioate

1.2 Other means of identification

Product number -
Other names Phenyl allyldithiocarbamate

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:62118-13-2 SDS

62118-13-2Relevant academic research and scientific papers

Multicomponent Synthesis of Biologically Relevant S-Aryl Dithiocarbamates Using Diaryliodonium Salts

Parida, Sushanta K.,Jaiswal, Sonal,Singh, Priyanka,Murarka, Sandip

supporting information, p. 6401 - 6406 (2021/08/18)

A transition-metal-free one-pot three-component annulation between diaryliodonium triflates, cyclic and acyclic aliphatic amines, and carbon disulfide providing a convenient and efficient access to biologically relevant S-aryl dithiocarbamates is developed. The reaction does not require metal, base, or any other additive and operates under mild and ambient conditions. This methodology is robust, scalable, and exhibits a broad substrate scope. The in silico analysis revealed that the majority of the compounds have a drug-likeness and good ADMET characteristics.

Manganese dioxide in a new role of Sulfur extrusion in thioamides

Radha Rani,Rahman,Bhalerao

, p. 1953 - 1958 (2007/10/02)

A simple and efficient procedure for the mild conversion of thioamides to amides in good yields using active manganese dioxide is described.

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