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75755-45-2

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75755-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75755-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,5 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75755-45:
(7*7)+(6*5)+(5*7)+(4*5)+(3*5)+(2*4)+(1*5)=162
162 % 10 = 2
So 75755-45-2 is a valid CAS Registry Number.

75755-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,2-dimethyl-N-phenylpropanethioamide

1.2 Other means of identification

Product number -
Other names N,2-dimethylpropionthioanilid

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:75755-45-2 SDS

75755-45-2Relevant articles and documents

Preference of cis-Thioamide Structure in N-Thioacyl- N-methylanilines

Zhang, Jin,Liu, Zhulin,Yin, Zheng,Yang, Xiufang,Ma, Yangmin,Szostak, Roman,Szostak, Michal

supporting information, p. 9500 - 9505 (2020/12/21)

The thioamide group represents a highly attractive isostere of the amide bond. We report a combined structural and computational study on cis-thioamide conformation of N-thioacyl-N-methylanilines. Amide to thioamide replacement in a class of anilides that

2,4-Bis(4-methylphenylthio)-1,3,2λ5,4λ5-dithiadiphosphetane-2,4-dithione: A New Reagent for Thiation of N,N-Disubstituted Amides

Wipf, Peter,Jenny, Christjohannes,Heimgartner, Heinz

, p. 1001 - 1011 (2007/10/02)

As a new reagent for the thiation of amides, the easily accessible 2,4-bis(4-methylphenylthio)-1,3,2λ5,4λ5-dithiadiphosphetane-2,4-dithione (9) shows a remarkable selectivity.This selectivity - the preferred thiation of N,N-disubstituted amides - is complementary to the one of the well known Lawesson reagent.Thiation of diamides of type 2 with 9 leads via cyclization of the corresponding dithiodiamides directly to 1,3-thiazole-5(4H)-thiones 1.

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