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Cyclohexanecarbothioamide, 2-oxo-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20368-65-4

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20368-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20368-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,6 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20368-65:
(7*2)+(6*0)+(5*3)+(4*6)+(3*8)+(2*6)+(1*5)=94
94 % 10 = 4
So 20368-65-4 is a valid CAS Registry Number.

20368-65-4SDS

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 2-oxo-N-phenylcyclohexane-1-carbothioamide

1.2 Other means of identification

Product number -
Other names 2-oxo-cyclohexan-1-carbothionic acid anilide

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:20368-65-4 SDS

20368-65-4Relevant academic research and scientific papers

Synthesis of sulfanylidene-diazaspirocycloalkanones in a three-component Mannich-type reaction catalyzed with lactic acid

Jagodziński, Tadeusz S.,So?nicki, Jacek G.,Struk, ?ukasz

, p. 43 - 57 (2017/07/26)

The aminomethylation of thioamides containing an acidic hydrogen atom at the a-carbon atom was investigated as a general reaction. Spirohexahydropyrimidines were obtained in the one-pot, three-component reaction of a variety of cyclic-ketone-derived thioamides, primary amines and formaldehyde with lactic acid acting as a catalyst. The results of our experiments confirmed the high catalytic efficiency of lactic acid. A proper choice of the starting thioamides and amines makes it possible to use this reaction methodolgy to synthesize several new and potentially useful derivatives of hexahydropyrimidine, e.g., biologically-active compounds.

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