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Benzenecarbothioamide, N-[(4-methoxyphenyl)-4-morpholinylmethylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91850-61-2

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91850-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91850-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,5 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91850-61:
(7*9)+(6*1)+(5*8)+(4*5)+(3*0)+(2*6)+(1*1)=142
142 % 10 = 2
So 91850-61-2 is a valid CAS Registry Number.

91850-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-((4-methoxyphenyl)(morpholino)methylene)benzothioamide

1.2 Other means of identification

Product number -
Other names -

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:91850-61-2 SDS

91850-61-2Upstream product

91850-61-2Relevant academic research and scientific papers

The Triethylamine Catalyzed Reaction of N,N-Disubstituted Thioamide-Bromine Adducts With Unsubstituted Thiobenzamide

Corsaro, Antonino,Compagnini, Anna,Perrini, Giancarlo,Purrello, Giovanni

, p. 897 - 900 (1984)

The reaction of N,N-disubstituted thioamide-bromine adducts with unsubstituted thioamide, followed by treatment with triethylamine, affords novel N'-thiobenzoylamidines along with smaller amounts of secondary products.A mechanism is proposed for the formation of the amidines.The results give an insight into the initial steps of the mechanism by which thioamides are converted into 1,2,4-thiadiazoles.

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