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53406-41-0

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53406-41-0 Usage

Derivative of

Indole

Also known as

Tryptamine

Found in

Plants and natural products

Psychoactive effects

Identified as a component in certain hallucinogenic substances

Research interest

Potential pharmaceutical and therapeutic applications

Potential applications

Treatment of psychiatric and neurological disorders

Risks

Associated with potential risks and adverse effects when used irresponsibly or in high doses.

Check Digit Verification of cas no

The CAS Registry Mumber 53406-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53406-41:
(7*5)+(6*3)+(5*4)+(4*0)+(3*6)+(2*4)+(1*1)=100
100 % 10 = 0
So 53406-41-0 is a valid CAS Registry Number.

53406-41-0SDS

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-methylindol-1-amine

1.2 Other means of identification

Product number -
Other names 1H-Indol-1-amine,2-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:53406-41-0 SDS

53406-41-0Upstream product

53406-41-0Relevant articles and documents

Synthesis of 1-amino-2-methylindoline by Raschig process: Parallel reactions, modeling, and optimization

Elkhatib,Peyrot,Metz,Tenu,Elomar,Delalu

, p. 575 - 584 (2002)

The reaction between chloramine and 2-methylindoline was studied at pH 12.89, T = 40°C, and for different initial concentrations of reactants. The interaction includes two concurrent bimolecular mechanisms leading to 1-amino-2-methylindoline and 2-methyli

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