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Methanethioamide, N,N-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25576-20-9

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25576-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25576-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,7 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25576-20:
(7*2)+(6*5)+(5*5)+(4*7)+(3*6)+(2*2)+(1*0)=119
119 % 10 = 9
So 25576-20-9 is a valid CAS Registry Number.

25576-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dibenzylmethanethioamide

1.2 Other means of identification

Product number -
Other names dibenzylthioformamide

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:25576-20-9 SDS

25576-20-9Relevant academic research and scientific papers

Kulinkovich-type reactions of thioamides: Similar to those of carboxylic amides?

Augustowska, Ewelina,Boiron, Antoine,Deffit, Jerome,Six, Yvan

experimental part, p. 5031 - 5033 (2012/06/01)

The behaviour of thioamides under Kulinkovich-type conditions is compared with the known reactivity of carboxylic amides. Dramatic differences are disclosed. The Royal Society of Chemistry 2012.

Direct thionation and selenation of amides using elemental sulfur and selenium and hydrochlorosilanes in the presence of amines

Shibahara, Fumitoshi,Sugiura, Rie,Murai, Toshiaki

supporting information; experimental part, p. 3064 - 3067 (2009/12/05)

Reactions of amides with elemental sulfur in the presence of hydrochlorosilanes and amines give the corresponding thioamides in good to high yields. The process takes place via reduction of elemental sulfur by the hydrochlorosilane in the presence of a suitable amine. The methodology can be applied to the selenation of amides by using elemental selenium. Thlonation and selenation of an acetyl-protected sialic acid derivative are found to take place selectively at the amide group.

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