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4-methyl-N1-phenylbenzene-1,3-diamine, also known as 4-Methyl-N-phenyl-1,3-benzenediamine or 4-Methyl-N-phenylbenzene-1,3-diamine, is an organic compound with the chemical formula C14H14N2. It is a derivative of benzene-1,3-diamine, featuring a methyl group at the 4-position and a phenyl group attached to the nitrogen at the 1-position. 4-methyl-N1-phenylbenzene-1,3-diamine is a white to off-white crystalline solid and is used as an intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. It is also known for its potential applications in the production of hair dyes and as a building block for more complex organic molecules. Due to its reactivity and the presence of amine groups, it is important to handle this chemical with care, as it can react with a variety of substances and may have specific safety considerations.

6406-71-9

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6406-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6406-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6406-71:
(6*6)+(5*4)+(4*0)+(3*6)+(2*7)+(1*1)=89
89 % 10 = 9
So 6406-71-9 is a valid CAS Registry Number.

6406-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1-N-phenylbenzene-1,3-diamine

1.2 Other means of identification

Product number -
Other names 3-Amino-4-methyl-diphenylamin

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:6406-71-9 SDS

6406-71-9Relevant academic research and scientific papers

Intermolecular Reductive C-N Cross Coupling of Nitroarenes and Boronic Acids by PIII/PV=O Catalysis

Nykaza, Trevor V.,Cooper, Julian C.,Li, Gen,Mahieu, Nolwenn,Ramirez, Antonio,Luzung, Michael R.,Radosevich, Alexander T.

supporting information, p. 15200 - 15205 (2018/11/30)

A main group-catalyzed method for the synthesis of aryl- and heteroarylamines by intermolecular C-N coupling is reported. The method employs a small-ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane) and a terminal hydrosilane reductant (phenylsilane) to drive reductive intermolecular coupling of nitro(hetero)arenes with boronic acids. Applications to the construction of both Csp2-N (from arylboronic acids) and Csp3-N bonds (from alkylboronic acids) are demonstrated; the reaction is stereospecific with respect to Csp3-N bond formation. The method constitutes a new route from readily available building blocks to valuable nitrogen-containing products with complementarity in both scope and chemoselectivity to existing catalytic C-N coupling methods.

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