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"Benzenamine, N-(1-oxido-2-phenyl-3H-indol-3-ylidene)-" is a complex organic chemical compound with the molecular formula C17H12N2O. It is a derivative of benzenamine (aniline), where the amino group is bonded to a 1-oxido-2-phenyl-3H-indol-3-ylidene moiety. Benzenamine, N-(1-oxido-2-phenyl-3H-indol-3-ylidene)- is characterized by its unique structure, which features a benzene ring, an indole ring, and an oxidized nitrogen atom. It is an important intermediate in the synthesis of various pharmaceuticals and dyes due to its versatile chemical properties and reactivity. The compound is typically synthesized through various chemical reactions, such as condensation or substitution, and is used in the preparation of more complex molecules with potential applications in the fields of medicine, agriculture, and materials science.

5165-73-1

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5165-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5165-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,6 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5165-73:
(6*5)+(5*1)+(4*6)+(3*5)+(2*7)+(1*3)=91
91 % 10 = 1
So 5165-73-1 is a valid CAS Registry Number.

5165-73-1SDS

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 1-oxido-N,2-diphenylindol-1-ium-3-imine

1.2 Other means of identification

Product number -
Other names Benzenamine,N-(1-oxido-2-phenyl-3H-indol-3-ylidene)

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:5165-73-1 SDS

5165-73-1Relevant academic research and scientific papers

Direct Amination. Part 2. Reaction of 2-Phenylindole with Primary Aromatic Amines. A Chemical and Electrochemical Investigation

Berti, Corrado,Greci, Lucedio,Andruzzi, Romano,Trazza, Antonio

, p. 607 - 610 (2007/10/02)

The reaction of 2-phenylindole with primary aromatic amines to form 2-phenyl-3-arylimino-3H-indoles, in the presence of N-chlorobenzotriazole, N-chloroisatin or lead tetraacetate, were also investigated by anodic oxidation.The chemical and electrochemical results suggest a mechanism involving an intermediate nitrenium ion, whose formation was demonstrated by an independent route.The reaction of 1-hydroxy-2-phenylindole with p-anisidine to form 2-phenyl-3-p-methoxyphenylimino-3H-indole 1-oxide, previously studied under anodic oxidation is here described in the presence of N-chlorobenzotriazole.

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