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N-(5-bromobiphenyl-2-yl)benzamide is a chemical compound with the molecular formula C13H10BrNO. It is a derivative of benzamide, featuring a 5-bromobiphenyl-2-yl group attached to the nitrogen atom. N-(5-bromobiphenyl-2-yl)benzamide is characterized by its aromatic structure, with a bromine atom at the 5-position of the biphenyl ring, which influences its electronic properties and reactivity. It is a white crystalline solid and is often used in organic synthesis and as an intermediate in the production of pharmaceuticals and other specialty chemicals. The presence of the bromine atom makes it a potential candidate for further functionalization or as a precursor in the synthesis of more complex molecules.

7511-41-3

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7511-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7511-41-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7511-41:
(6*7)+(5*5)+(4*1)+(3*1)+(2*4)+(1*1)=83
83 % 10 = 3
So 7511-41-3 is a valid CAS Registry Number.

7511-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-ethylhexanoic acid

1.2 Other means of identification

Product number -
Other names 5-Brom-2-benzamino-diphenyl

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:7511-41-3 SDS

7511-41-3Downstream Products

7511-41-3Relevant academic research and scientific papers

Electrochemical Synthesis of Carbazoles by Dehydrogenative Coupling Reaction

Kehl, Anton,Schupp, Niclas,Breising, Valentina M.,Schollmeyer, Dieter,Waldvogel, Siegfried R.

supporting information, p. 15847 - 15851 (2020/11/02)

A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N-protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.

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