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1H-Indol-3-amine, 5-methyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23747-09-3

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23747-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23747-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,4 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23747-09:
(7*2)+(6*3)+(5*7)+(4*4)+(3*7)+(2*0)+(1*9)=113
113 % 10 = 3
So 23747-09-3 is a valid CAS Registry Number.

23747-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-phenyl-1H-indol-3-amine

1.2 Other means of identification

Product number -
Other names 5-Methyl-2-phenyl-3-aminoindole

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:23747-09-3 SDS

23747-09-3Relevant academic research and scientific papers

Synthesis of Substituted 1,2,3,8-Tetrahydroindolobenzodiazepin-2-ones and 5,6,7,8-Tetrahydroindolobenzodiazepin-6-ones

Hiremath, Shivayogi P.,Badami, Prema S.,Purohit, Muralidhar G.

, p. 1115 - 1119 (2007/10/02)

Nitrosation (NaNO2/AcOH) of 2-phenylindoles (1a-d) and subsequent reduction of the resultant 3-nitroso-2-phenylindoles (2a-d) with sodium dithionite in alkali furnish the corresponding 3-aminoindoles (3a-d), which on condensation with ethyl chloroformate

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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