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61021-51-0

61021-51-0

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61021-51-0 Usage

Chemical Properties

White Waxy Crystals

Uses

(Indol-3-ylthio)acetonitrile (cas# 61021-51-0) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 61021-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,2 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61021-51:
(7*6)+(6*1)+(5*0)+(4*2)+(3*1)+(2*5)+(1*1)=70
70 % 10 = 0
So 61021-51-0 is a valid CAS Registry Number.

61021-51-0SDS

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 2-(1H-indol-3-ylsulfanyl)acetonitrile

1.2 Other means of identification

Product number -
Other names Acetonitrile,(1H-indol-3-ylthio)

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:61021-51-0 SDS

61021-51-0Relevant articles and documents

A tetra-: N -butylammonium iodide mediated reaction of indoles with Bunte salts: Efficient 3-sulfenylation of indoles under metal-free and oxidant-free conditions

Li, Jian,Cai, Zhong-Jian,Wang, Shun-Yi,Ji, Shun-Jun

supporting information, p. 9384 - 9387 (2016/10/13)

A highly efficient tetra-n-butylammonium iodide (TBAI) triggered procedure for 3-sulfenylation of indoles with Bunte salts is demonstrated. This protocol provides a simple strategy to prepare 3-alkylthioindoles and 3-arylthioindoles from the corresponding indoles under metal-free and oxidant-free conditions.

Substituted indoles

-

, (2008/06/13)

Substituted thioindoles and their sulfoxide and sulfone derivatives, useful as cardiac rate lowering agents and for other pharmacological properties, and precursors therefor.

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