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61021-66-7

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61021-66-7 Usage

Chemical structure

2-[(2-Methyl-1H-indol-3-yl)thio]ethanamine consists of a thioether functional group and an amine group.

Usage

It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds.

Biological activity

2-[(2-Methyl-1H-indol-3-yl)thio]ethanamine has potential biological activity and has been studied for its potential medicinal applications.

Role in synthesis

The compound is known for its role in the synthesis of various organic compounds.

Chemical reagent

2-[(2-Methyl-1H-indol-3-yl)thio]ethanamine is used as a reagent in a variety of chemical reactions.

Importance in organic chemistry

It is an important compound in organic chemistry.

Potential applications

The compound has various potential applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 61021-66-7 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, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61021-66:
(7*6)+(6*1)+(5*0)+(4*2)+(3*1)+(2*6)+(1*6)=77
77 % 10 = 7
So 61021-66-7 is a valid CAS Registry Number.

61021-66-7SDS

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-[(2-methyl-1H-indol-3-yl)sulfanyl]ethanamine

1.2 Other means of identification

Product number -
Other names F1386-0286

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:61021-66-7 SDS

61021-66-7Downstream Products

61021-66-7Relevant articles and documents

Cardiac-Slowing Amidines Containing the 3-Thioindole Group. Potential Antianginal Agents

Zelesko, Michael J.,McComsey, David F.,Hageman, William E.,Nortey, Samuel O.,Baker, Carol A.,Maryanoff, Bruce E.

, p. 230 - 237 (2007/10/02)

A series of 3-thioindolamidines (and 3-indolamidines) related to mixidine (1) was studied for cardiac-slowing properties, allowing the discovery of activity for prototype thioindole 2.Structure-activity relationships were explored, leading to many potent antitachycardic agents (6-9, 12, 13, 15-17, 20, 23, 24, 30, 34, 35, 45, and 47-49).Relative to 2, cardiac-slowing activity is enhanced by substitution of the indole nitrogen with small (C1-C3) saturated alkyl groups (6-9), unsaturated alkyl groups (12, 13, and 15-17), or a methoxyethyl group (20); replacement of the N-methyl group with alkyl (23) or phenyl groups (24); and extension of the ethylene bridge by two methylene units (34).Dethio (i.e., 3-indole) analogues of 2 with alkyl substitution on the indole nitrogen (47-49) have greater activity as well.Several potent compounds were also found to have minimal myocardial depression (6-9, 13, 45, and 47).Secondary pharmacological testing is reported for thioindoles 2, 6, 7, 9, and 28.

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