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2-Phenylindol-3-imine is an organic compound with the molecular formula C14H10N2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a phenyl group attached to the 2-position and an imine functional group at the 3-position. 2-phenylindol-3-imine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of dyes and pigments. The imine group in 2-phenylindol-3-imine can participate in various chemical reactions, such as reduction, hydrolysis, and condensation, making it a versatile building block in organic synthesis.

6339-33-9

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6339-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6339-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6339-33:
(6*6)+(5*3)+(4*3)+(3*9)+(2*3)+(1*3)=99
99 % 10 = 9
So 6339-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9,15H/b15-13+

6339-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylindol-3-imine

1.2 Other means of identification

Product number -
Other names 3-Imino-2-phenylindolenon

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:6339-33-9 SDS

6339-33-9Relevant academic research and scientific papers

ACYLHYDRAZONES OF 3H-INDOL-3-ONE

Berdinskii, I. S.,Maslivets, A. N.,Orlova, L. D.

, p. 814 - 816 (2007/10/02)

The reaction of 3-ethoxalyl- and acetylhydrazones of isatin with arylmagnesium bromide leads to the glycoloyl- and acetylhydrazones of 2-aryl-3H-indol-3-one as a result of the participation of the α-carbonyl group of the isatin ring in the reaction.

Synthesis and Reactions of 2-Phenylindol-3-ones

Hiremath, Shivayogi P.,Biradar, Jaiprakash S.,Mruthyunjayaswamy, B. H. M.

, p. 308 - 310 (2007/10/02)

2-Phenyl-3-aminoindoles (2a-d) have been synthesised and converted into the corresponding 2-phenylindol-3-ones (4a-d), which on reaction with o-phenylenediamine (5a,b) and nitrostyrene give 9-substituted 5H-5a,6-dihydro-5a-phenylindoloquinoxalines

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