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2-(2-METHYL-1-PHENYL-1H-INDOL-3-YL)-ETHYLAMINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

692739-71-2

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692739-71-2 Usage

Chemical class

Aralkylamines, which are alkylamines with an aromatic hydrocarbon group substitution on one carbon atom.

Physical appearance

White solid, which describes the color and form of the compound when it is not dissolved in any solvent.

Potential applications

As a psychoactive drug with potential antidepressant and mood-enhancing properties, which suggests its possible use in treating mental health disorders like depression and anxiety.

Current status

Primarily used in scientific research and pharmaceutical development, which highlights its ongoing investigation for potential therapeutic uses.

Need for further research

Additional studies and clinical trials are required to determine the safety and efficacy of 2-(2-METHYL-1-PHENYL-1H-INDOL-3-YL)-ETHYLAMINE HYDROCHLORIDE for the treatment of mental health disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 692739-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,7,3 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 692739-71:
(8*6)+(7*9)+(6*2)+(5*7)+(4*3)+(3*9)+(2*7)+(1*1)=212
212 % 10 = 2
So 692739-71-2 is a valid CAS Registry Number.

692739-71-2Downstream Products

692739-71-2Relevant academic research and scientific papers

Efficient one-pot synthesis of tryptamines and tryptamine homologues by amination of chloroalkynes

Khedkar, Vivek,Tillack, Annegret,Michalik, Manfred,Beller, Matthias

, p. 3123 - 3126 (2007/10/03)

A new method was developed for the one-pot synthesis of substituted 3-(2-aminoethyl)- and 3-(3-aminopropyl)indoles from commercially available aryl hydrazines and chloroalkylalkynes. Various tryptamine derivatives were prepared directly in good yield with excellent regioselectivity. The method involves a new domino reaction sequence consisting of a titanium-catalyzed amination of the chloroalkylalkyne, [3+3]-rearrangement of the resulting aryl hydrazone, and nucleophilic substitution of the chloride by ammonia.

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