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N-[4-benzamido-2-(benzenesulfonyl)phenyl]benzamide is a complex organic compound with the molecular formula C24H18N2O4S. It is characterized by a benzamide group attached to a phenyl ring, which in turn is connected to another benzene ring through a sulfonyl group. The compound features a 4-benzamido group and a 2-benzenesulfonyl group, which contribute to its unique chemical properties. This molecule is of interest in the field of organic chemistry, potentially for its reactivity or as a building block in the synthesis of more complex molecules. Its specific applications may vary, but it could be relevant in pharmaceuticals, materials science, or as an intermediate in chemical synthesis.

6334-58-3

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6334-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6334-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6334-58:
(6*6)+(5*3)+(4*3)+(3*4)+(2*5)+(1*8)=93
93 % 10 = 3
So 6334-58-3 is a valid CAS Registry Number.

6334-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-benzamido-3-(benzenesulfonyl)phenyl]benzamide

1.2 Other means of identification

Product number -
Other names N,N'-(benzenesulfonyl-p-phenylene)-bis-benzamide

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:6334-58-3 SDS

6334-58-3Relevant academic research and scientific papers

Reaction of N,N′-disubstituted 1,4-benzoquinone diimines with sodium arenesulfinates

Konovalova,Avdeenko,Santalova,Palamarchuk,D'Yakonenko,Shishkin

, p. 42 - 50 (2015/03/04)

Radical anion 1,6-addition path in the reactions of N,N′-disubstituted 1,4-benzoquinone diimines with sodium arenesulfinates is favored by increase of the electron-donating power of the substituent in the para position of arenesulfinate ion and redox pote

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