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2-(2-Benzoylphenyl)benzoic acid is a complex organic compound with the chemical formula C20H14O4. It is a white crystalline solid that belongs to the class of benzoic acids, characterized by the presence of a benzoyl group (C6H5-CO-) attached to a phenyl ring. 2-(2-benzoylphenyl)benzoic acid is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure. It is also used as an intermediate in the production of certain dyes and pigments. The compound's molecular structure features two benzene rings, one of which is further connected to a benzoic acid group, while the other is linked to a benzoyl group, creating a conjugated system that can influence its chemical properties and reactivity.

6630-85-9

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6630-85-9 Usage

Physical appearance

White to off-white crystalline powder

Melting point

282-284 degrees Celsius

Usage in pharmaceutical research

Intermediate for the synthesis of various biologically active compounds

Potential applications

Pharmaceutical ingredient (cancer cell growth inhibition, anti-inflammatory properties)

Industrial applications

Production of organic pigments and dyes

Diverse potential applications

Pharmaceutical and industrial settings

Check Digit Verification of cas no

The CAS Registry Mumber 6630-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6630-85:
(6*6)+(5*6)+(4*3)+(3*0)+(2*8)+(1*5)=99
99 % 10 = 9
So 6630-85-9 is a valid CAS Registry Number.

6630-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-benzoylphenyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2'-benzoyl-biphenyl-2-carboxylic acid

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:6630-85-9 SDS

6630-85-9Relevant academic research and scientific papers

Developments in Meyers' lactamization methodology: En route to Bi(hetero)aryl structures with defined axial chirality

Postikova, Svetlana,Sabbah, Mohamad,Wightman, Daniel,Nguyen, Ich Tuan,Sanselme, Morgane,Besson, Thierry,Briere, Jean-Francois,Oudeyer, Sylvain,Levacher, Vincent

supporting information, p. 8191 - 8197 (2013/09/12)

Highly atroposelective Meyers' lactamization promoted by pivalic acid under microwave irradiation is reported which allows the construction of nonracemic substituted-dibenzo(di)azepine derivatives through a center to axial chirality transfer principle, controlling the otherwise configurationally labile biaryl axis. This approach provides a straightforward entry to enantioenriched analogues of biorelevant architectures.

Therapeutic and diagnostic ligand systems comprising transport molecule binding properties and medicaments containing the same

-

, (2008/06/13)

The invention relates to transport molecule binding ligand compounds which comprise a therapeutically and/or diagnostically active substance and a carrier molecule-affine substance with a high association constant to the carrier molecule. The invention also relates to medicaments containing these ligand compounds and to diagnostic kits.

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