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10022-76-1

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10022-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10022-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10022-76:
(7*1)+(6*0)+(5*0)+(4*2)+(3*2)+(2*7)+(1*6)=41
41 % 10 = 1
So 10022-76-1 is a valid CAS Registry Number.

10022-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(1H-indol-3-yl)ethyl]-2-phenylethanethioamide

1.2 Other means of identification

Product number -
Other names N-<2-(3-Indolyl)-ethyl>-phenylthioacetamid

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:10022-76-1 SDS

10022-76-1Downstream Products

10022-76-1Relevant articles and documents

Method for synthesizing thioamide compound from 1,2,3-thiodiazole compound and amine under catalysis of copper

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Paragraph 0140-0146, (2021/05/12)

The invention belongs to the technical field of organic chemistry, and discloses a method for synthesizing a thioamide compound from a 1,2,3-thiodiazole compound and amine under the catalysis of copper. The method comprises the following steps: in a protective atmosphere, taking an organic solvent as a reaction medium, reacting a 1,2,3-thiodiazole compound with an amine compound under the action of a copper salt catalyst or a copper catalyst and a phosphine ligand, and carrying out subsequent treatment to obtain the thioamide compound. According to the method, the copper salt is used as the catalyst, the phosphine ligand is adopted, the yield is high, and the substrate applicability is wide. In addition, the reaction takes the 1,2,3-thiodiazole compound and the amine compound as raw materials, and has the advantages that the raw materials are cheap and easy to prepare, the operation is simple and convenient, and the atom economy is high.

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