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N-(4-bromophenyl)pentanethioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35274-23-8

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35274-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35274-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,7 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35274-23:
(7*3)+(6*5)+(5*2)+(4*7)+(3*4)+(2*2)+(1*3)=108
108 % 10 = 8
So 35274-23-8 is a valid CAS Registry Number.

35274-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-bromophenyl)pentanethioamide

1.2 Other means of identification

Product number -
Other names N-p-Bromphenyl-thiovaleramid

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:35274-23-8 SDS

35274-23-8Downstream Products

35274-23-8Relevant academic research and scientific papers

Lewis Base-Boryl Radicals Enabled the Desulfurizative Reduction and Annulation of Thioamides

Yu, You-Jie,Zhang, Feng-Lian,Cheng, Jie,Hei, Jing-Hao,Deng, Wei-Ting,Wang, Yi-Feng

supporting information, p. 24 - 27 (2018/01/17)

A new protocol for radical transformations of thioamides promoted by Lewis base-boryl radicals is reported. The desulfurizative reduction to access organic amines was enabled utilizing 4-dimethylaminopyridine-BH3 as the boryl radical precursor and PhSH as the polarity reversal catalyst. Alternatively, the chain process for unsaturated thioamides was switched to an annulation reaction using N-heterocyclic carbene-BH3 as the boryl radical precursor and sterically bulky Ph3CSH as the catalyst, allowing for the construction of N-heterocyclic and carbocyclic skeletons.

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