149817-31-2 Usage
Chemical Class
2-(3,5-dimethylbenzoyl)benzoic acid belongs to the class of benzoylbenzoic acids.
Physical Appearance
The compound is a white crystalline solid.
Solubility
It is sparingly soluble in water but more soluble in organic solvents such as ethanol and ether.
Chemical Structure
The structure consists of a benzoyl group attached to a benzoic acid group, with two methyl groups located on the benzene ring.
Versatile Chemical Properties
2-(3,5-dimethylbenzoyl)benzoic acid has versatile chemical properties, making it commonly used in the synthesis of various pharmaceuticals and organic molecules.
Building Block
The compound is a valuable building block in the field of organic chemistry.
Applications
2-(3,5-dimethylbenzoyl)benzoic acid has various applications in the production of drugs, dyes, and other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 149817-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,8,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 149817-31:
(8*1)+(7*4)+(6*9)+(5*8)+(4*1)+(3*7)+(2*3)+(1*1)=162
162 % 10 = 2
So 149817-31-2 is a valid CAS Registry Number.
149817-31-2Relevant articles and documents
Decarboxylative C-H arylation of benzoic acids under radical conditions
Seo, Sangwon,Slater, Mark,Greaney, Michael F.
supporting information; scheme or table, p. 2650 - 2653 (2012/07/27)
A decarboxylative radical cyclization reaction has been developed for the synthesis of fluorenones. The reaction uses Ag(I)/K2S 2O8 to oxidatively decarboxylate an aroylbenzoic acid to an aryl radical, which undergoes cyclization to afford fluorenone products in good yield.
