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C-(2,3-DIMETHYL-1H-INDOL-5-YL)-METHYLAMINE, also known as 5,7-dimethyl-1H-indole-6-methanamine, is a chemical compound with the molecular formula C11H15N. It is an aromatic amine derivative with a substituted indole structure, containing a methylamine group attached to the indole ring. C-(2,3-DIMETHYL-1H-INDOL-5-YL)-METHYLAMINE is known for its unique structure and reactivity, making it a versatile building block in organic chemistry reactions and a component in the synthesis of pharmaceuticals and other organic compounds. It also exhibits biological activity in certain biochemical processes.

5054-94-4

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5054-94-4 Usage

Uses

Used in Pharmaceutical Synthesis:
C-(2,3-DIMETHYL-1H-INDOL-5-YL)-METHYLAMINE is used as a key intermediate in the synthesis of various pharmaceuticals due to its unique structure and reactivity. It contributes to the development of new drugs by providing a foundation for chemical reactions that can lead to the creation of medicinal compounds.
Used in Organic Chemistry Reactions:
As a building block in organic chemistry, C-(2,3-DIMETHYL-1H-INDOL-5-YL)-METHYLAMINE is used in a variety of chemical reactions to form a range of organic compounds. Its aromatic amine and substituted indole structure allow it to participate in numerous synthetic pathways, making it valuable for the production of specialty chemicals and complex organic molecules.
Used in Biochemical Research:
C-(2,3-DIMETHYL-1H-INDOL-5-YL)-METHYLAMINE is utilized in biochemical research for its biological activity. It can be employed in studies to understand its interactions with biological systems, potentially leading to insights into new therapeutic targets or mechanisms of action for drug development.
Used in Industrial Applications:
In industrial settings, C-(2,3-DIMETHYL-1H-INDOL-5-YL)-METHYLAMINE may be used as a precursor or component in the production of various chemical products. Its versatility and reactivity make it suitable for a range of applications, from the synthesis of dyes and pigments to the creation of advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 5054-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,5 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5054-94:
(6*5)+(5*0)+(4*5)+(3*4)+(2*9)+(1*4)=84
84 % 10 = 4
So 5054-94-4 is a valid CAS Registry Number.

5054-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3-dimethyl-1H-indol-5-yl)methanamine

1.2 Other means of identification

Product number -
Other names 5-Aminomethyl-2,3-dimethylindol

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:5054-94-4 SDS

5054-94-4Downstream Products

5054-94-4Relevant academic research and scientific papers

SYNTHESIS OF BENZO(AMINOMETHYL)INDOLES

Muminov, A.,Yudin, L. G.,Zinchenko, E. Ya.,Romanova, N. N.,Kost, A. N.

, p. 1012 - 1015 (2007/10/02)

The benzene ring in indoles has been aminomethylated in high yield by reaction with methylolphtalimide followed by hydrazinolysis of the phtalimidomethyl derivatives.In the hydrazinolysis of one of the phtalimidomethyl compounds, an intermediate product (the amino-methylindole phtalazine) was isolated and characterized.

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