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1H-Indol-1-amine, 3-phenyl-, also known as 3-phenylindole or 3-phenyl-1H-indole, is an organic compound with the molecular formula C14H12N. It is a derivative of indole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a pyrrole ring. The phenyl group is attached to the indole nucleus at the 3-position, which is the carbon atom adjacent to the nitrogen atom in the pyrrole ring. 1H-Indol-1-amine, 3-phenyl- is an important building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. It is also used as an intermediate in the preparation of indole-based natural products and has potential applications in materials science and chemical research.

3929-81-5

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3929-81-5 Usage

Chemical class

Indoles (organic compounds)

Physical form

Crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

Synthesis of pharmaceuticals, agrochemicals, and dyes

Biological activity

Studied for potential applications in medicine and industry

Handling precautions

May pose health hazards if not handled properly

Check Digit Verification of cas no

The CAS Registry Mumber 3929-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3929-81:
(6*3)+(5*9)+(4*2)+(3*9)+(2*8)+(1*1)=115
115 % 10 = 5
So 3929-81-5 is a valid CAS Registry Number.

3929-81-5SDS

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 3-phenylindol-1-amine

1.2 Other means of identification

Product number -
Other names 3-phenyl-indol-1-ylamine

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:3929-81-5 SDS

3929-81-5Relevant academic research and scientific papers

Planarized Intramolecular Charge Transfer: A Concept for Fluorophores with both Large Stokes Shifts and High Fluorescence Quantum Yields

Haberhauer, Gebhard,Gleiter, Rolf,Burkhart, Christoph

, p. 971 - 978 (2016)

Fluorophores were successfully used in several areas of chemistry and biochemistry. For many purposes, however, it is necessary that the fluorescence compound features a high fluorescence quantum yield as well as a large Stokes shift. The latter is, for e

1-Amino-3-phenylindoles with antidepressant activity. Binodaline hydrochloride and related substances

Schatz,Jahn,Wagner-Jauregg,Zirngibl,Thiele

, p. 919 - 923 (2007/10/02)

From a number of novel N-alkylated derivatives of 1-amino-3-phenyl-indole tested as tetrabenzaine antagonists, binodaline hydrochloride has been selected as a potential antidepressant substance for clinical trials. The structure of the side chain is compared to that of known tricyclic antidepressants.

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