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C-(6,7,8,9-Tetrahydro-5H-carbazol-3-yl)-methylamine is a chemical compound with the molecular formula C14H17N. It is a derivative of carbazole, a tricyclic aromatic hydrocarbon, featuring a methylamine group attached to the carbazole ring. This unique structure endows it with distinctive chemical properties and reactivity, making it a valuable building block in organic synthesis. Its potential applications span across pharmaceuticals, material science, and as a fluorescent dye, highlighting its versatility in various scientific and industrial domains.

76061-94-4

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76061-94-4 Usage

Uses

Used in Pharmaceutical Synthesis:
C-(6,7,8,9-Tetrahydro-5H-carbazol-3-yl)-methylamine is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used in Drug Discovery and Development:
Due to its pharmacological properties, C-(6,7,8,9-Tetrahydro-5H-carbazol-3-yl)-methylamine serves as a promising candidate in drug discovery and development. Researchers leverage its chemical reactivity to create novel compounds with potential medicinal applications.
Used in Material Science:
In the field of material science, C-(6,7,8,9-Tetrahydro-5H-carbazol-3-yl)-methylamine has been studied for its potential applications. Its unique properties may contribute to the development of new materials with specific characteristics for various uses.
Used as a Fluorescent Dye:
C-(6,7,8,9-Tetrahydro-5H-carbazol-3-yl)-methylamine has also been investigated for its potential as a fluorescent dye. Its optical properties could be harnessed in applications requiring fluorescence, such as in bioimaging or as markers in analytical chemistry.
Used in Organic Synthesis:
As a building block in organic synthesis, C-(6,7,8,9-Tetrahydro-5H-carbazol-3-yl)-methylamine is employed to construct a wide range of organic compounds. Its reactivity and structural features make it a versatile component in creating new chemical entities for various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 76061-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,6 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76061-94:
(7*7)+(6*6)+(5*0)+(4*6)+(3*1)+(2*9)+(1*4)=134
134 % 10 = 4
So 76061-94-4 is a valid CAS Registry Number.

76061-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7,8,9-tetrahydro-5H-carbazol-3-ylmethanamine

1.2 Other means of identification

Product number -
Other names 5,6,7,8,9-pentahydro-4aH-carbazol-3-ylmethylamine

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:76061-94-4 SDS

76061-94-4Downstream Products

76061-94-4Relevant 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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