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2-(2,5-dimethoxybenzoyl)benzoic acid is a complex organic compound with the molecular formula C16H14O6. It is a derivative of benzoic acid, featuring a benzene ring with a carboxyl group at the 2-position and a 2,5-dimethoxybenzoyl group attached to it. 2-(2,5-dimethoxybenzoyl)benzoic acid is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the development of drugs targeting the central nervous system. Its structure provides a foundation for further chemical modifications, making it a valuable component in medicinal chemistry research.

76526-29-9

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76526-29-9 Usage

Derived from

Benzoic acid

Functional groups

Carboxylic acid group, benzoyl group

Molecular structure

Benzene rings with methoxy groups attached

Versatility

Can be used in various chemical reactions

Potential applications

Drug development, organic synthesis

Reactivity

Unique structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 76526-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,2 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76526-29:
(7*7)+(6*6)+(5*5)+(4*2)+(3*6)+(2*2)+(1*9)=149
149 % 10 = 9
So 76526-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O5/c1-20-10-7-8-14(21-2)13(9-10)15(17)11-5-3-4-6-12(11)16(18)19/h3-9H,1-2H3,(H,18,19)

76526-29-9Relevant academic research and scientific papers

Intermediates for polycyclic quinonoid antibiotics

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, (2008/06/13)

There is provided a novel method of synthesizing certain tetracyclic quinones. In particular, there is provided a novel route to the synthesis of certain analogs of (+)-7-deoxydaunomycinone which includes the provision of novel tri- and tetracyclic quinone intermediates. The products of the synthetic route provided herein may be converted into compounds of known anti-neoplastic activity.

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