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13637-38-2

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13637-38-2 Usage

Structure

A derivative of indole

Usage

Commonly used as a reagent in organic synthesis

Biological Activities

a. Anti-inflammatory
b. Antiviral
c. Anticancer

Potential Applications

a. Development of new pharmaceutical drugs
b. Tool for understanding mechanisms of various biological processes

Use in Organic Chemistry

Building block for the synthesis of diverse chemical products

Check Digit Verification of cas no

The CAS Registry Mumber 13637-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,3 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13637-38:
(7*1)+(6*3)+(5*6)+(4*3)+(3*7)+(2*3)+(1*8)=102
102 % 10 = 2
So 13637-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NS/c1-10-8-5-3-2-4-7(8)6-9(10)11/h2-5H,6H2,1H3

13637-38-2SDS

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 1-methyl-3H-indole-2-thione

1.2 Other means of identification

Product number -
Other names 2H-Indole-2-thione,1,3-dihydro-1-methyl

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:13637-38-2 SDS

13637-38-2Relevant articles and documents

Synthesis of Tetrahydrothiopyrano[2,3-b]indole [60]Fullerene Derivatives via Hetero-Diels–Alder Reaction of C60 and α,β-Unsaturated Indole-2-thiones

Matloubi Moghaddam, Firouz,Ghanbari, Bahram,Behzadi, Masoumeh,Baghersad, Mohammad Hadi

, p. 911 - 915 (2017)

Hetero-Diels–Alder reactions of [60]fullerene with α,β-unsaturated thio-oxindoles (3a, 3b, 3c), prepared from thio-oxindole 1 and heteroaromatic aldehydes (2a, 2b, 2c), to generate tetrahydrothiopyrano[2,3-b]indole [60]fullerene cycloadducts (5a, 5b, 5c) under thermal or microwave irradiation were described. The yields were improved, and the reaction time was decreased by conducting the reaction under microwave irradiation.

Difluorocarbene-triggered cyclization: Synthesis of (hetero)arene-fused 2,2-difluoro-2,3-dihydrothiophenes

Liang, Huamin,Liu, Ran,Zhou, Min,Fu, Yue,Ni, Chuanfa,Hu, Jinbo

supporting information, p. 7047 - 7051 (2020/09/15)

An efficient method for the synthesis of (hetero)arene-fused 2,2-difluoro-2,3-dihydrothiophene derivatives using readily available sodium chlorodifluoroacetate (ClCF2CO2Na) has been developed. This transformation is achieved through a combination of a thi

Copper-catalyzed synthesis of 2-sulfenylindoles from indoline-2-thiones and aryl iodides

Zhou, Shiping,Xiao, Genhua,Liang, Yun

supporting information, p. 338 - 341 (2017/01/03)

A novel and efficient method for synthesis of 2-sulfenylindole via copper-catalyzed coupling reaction of indoline-2-thiones with aryl iodides has been developed. A series of N-substituted and N-free 2-sulfenylindole were obtained in high yields. Furthermo

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