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4-bromo-N-(4-bromo-2-methylphenyl)benzamide is a chemical compound with the molecular formula C14H11Br2NO. It is a derivative of benzamide, featuring a benzene ring with an amide functional group (-CO-NH2) attached to it. The compound is characterized by the presence of two bromine atoms, one attached to the benzene ring at the para position (4-bromo) and another one attached to the ortho position of the second benzene ring (4-bromo-2-methylphenyl). The second benzene ring also has a methyl group (-CH3) at the ortho position. 4-bromo-N-(4-bromo-2-methylphenyl)benzamide is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its use as an intermediate in chemical reactions. Due to its bromine substitutions, it may also be of interest in the study of halogenated aromatic compounds and their properties.

5306-59-2

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5306-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5306-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5306-59:
(6*5)+(5*3)+(4*0)+(3*6)+(2*5)+(1*9)=82
82 % 10 = 2
So 5306-59-2 is a valid CAS Registry Number.

5306-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-N-(4-bromo-2-methylphenyl)benzamide

1.2 Other means of identification

Product number -
Other names N-(4-bromo-2-methylphenyl)(4-bromophenyl)carboxamide

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

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More Details:5306-59-2 SDS

5306-59-2Downstream Products

5306-59-2Relevant academic research and scientific papers

Iron-catalyzed direct amination of azoles using formamides or amines as nitrogen sources in air

Wang, Jian,Hou, Ji-Ting,Wen, Jun,Zhang, Ji,Yu, Xiao-Qi

supporting information; experimental part, p. 3652 - 3654 (2011/05/02)

A new iron-catalyzed, direct C-H amination of azoles at C2 has been developed by using formamides or amines as nitrogen sources. Imidazole is the only additive in the catalyst system and oxygen in air is employed during the transformation process.

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