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5-Methoxy-1H-indol-3-methylamine, also known as MX, is a chemical compound belonging to the Indolamine family, specifically Tryptamines. It is found in some plants and fungi and is characterized by an indole structure, which consists 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 make it distinct from other indoles. As a specific Tryptamine, it possesses psychotropic properties, and its effects on the human nervous system have been a subject of scientific research. The stability, reactivity, and toxicological properties of this organic compound are continuously reviewed by chemists and biologists.

60523-82-2

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60523-82-2 Usage

Uses

Used in Pharmaceutical Research:
5-Methoxy-1H-indol-3-methylamine is used as a research compound for studying its psychotropic properties and potential effects on the human nervous system. Its unique structure and characteristics make it a valuable subject for understanding the interactions between chemical compounds and the nervous system.
Used in Chemical Synthesis:
5-Methoxy-1H-indol-3-methylamine is used as a starting material or intermediate in the synthesis of various organic compounds, particularly those with potential applications in the pharmaceutical and chemical industries. Its reactivity and stability under different conditions make it a useful component in the development of new chemical entities.
Used in Toxicological Studies:
5-Methoxy-1H-indol-3-methylamine is used as a test substance in toxicological research to evaluate its potential effects on living organisms and the environment. Understanding its toxicological properties is crucial for assessing its safety and potential risks associated with its use in various applications.
Used in Environmental Studies:
5-Methoxy-1H-indol-3-methylamine is used as a model compound in environmental studies to investigate its behavior and fate in different ecosystems. This helps in understanding the potential impact of such chemical compounds on the environment and developing strategies for their safe handling and disposal.
Used in Analytical Chemistry:
5-Methoxy-1H-indol-3-methylamine is used as a reference compound in analytical chemistry for the development and validation of analytical methods and techniques. Its unique properties make it a suitable candidate for testing the accuracy and precision of various analytical instruments and procedures.

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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