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60523-82-2

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60523-82-2 Usage

General Description

5-Methoxy-1H-indol-3-methylamine, also known as MX, is a chemical compound found in some plants and fungi. It belongs to the family of Indolamines, specifically Tryptamines. This organic compound is characterized by an indole, which is a stable element made of a benzene ring fused to a nitrogen-containing pyrrole ring. The Methoxy group (OCH3) on the 5th carbon and the Methylamine group (NH2CH3) on the 3rd carbon distinguishes it from other indoles. As a specific Tryptamine, it has psychotropic properties, and its effects on the human nervous system have been the subject of scientific research. The stability, reactivity, and toxicological properties of the substance under different environmental conditions continue to be reviewed by chemists and biologists.

Check Digit Verification of cas no

The CAS Registry Mumber 60523-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60523-82:
(7*6)+(6*0)+(5*5)+(4*2)+(3*3)+(2*8)+(1*2)=102
102 % 10 = 2
So 60523-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c1-13-8-2-3-10-9(4-8)7(5-11)6-12-10/h2-4,6,12H,5,11H2,1H3

60523-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-Methoxy-1H-indol-3-yl)methanamine

1.2 Other means of identification

Product number -
Other names (5-methoxy-1H-indol-3-yl)methanamine

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:60523-82-2 SDS

60523-82-2Relevant articles and documents

AN INTRAMOLECULAR PHOTOCYCLIZATION TO FORM THE AZEPINOINDOLE SYSTEM

Klohr, Steven E.,Cassady, John M.

, p. 671 - 674 (2007/10/02)

Azepinoindoles 5a and 5b are formed in good yield via the intramolecular photocyclization of N-chloroacetyl-3-aminomethylindoles.

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