1332524-02-3

Basic information

• Product Name: 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid
• Synonyms: 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid
• CAS NO: 1332524-02-3
• Molecular Weight: 241.219
• Mol File: 1332524-02-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid(1332524-02-3)
• EPA Substance Registry System: 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid(1332524-02-3)

Safety Data

• Hazardous Substances Data: 1332524-02-3(Hazardous Substances Data)

Usage

General Description

4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid is a chemical compound with the molecular formula C11H12FNO3. It is a derivative of benzoic acid and contains a carboxyl group, an amino group, and a fluorine atom. 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid is likely to have pharmaceutical applications due to its structure, as the presence of the carboxyl and amino groups suggests it may have biological activity. Additionally, the fluorine atom can enhance the compound's properties, making it potentially useful in drug development. Further research and testing would be necessary to fully understand the potential uses and effects of 4-(1-carboxyl-1-methylethylamino)-2-fluorobenzoic acid.

Upstream product

• 62-57-7 2-Aminoisobutyric acid 
• 112704-79-7 2-fluoro-4-bromobenzoic acid 
• 446-31-1 2-fluoro-4-aminobenzoic acid 
• 57-15-8 1,1,1-trichloro-2-methyl-2-propanol 

Downstream Products

• 1242137-15-0 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-imidazolidinethione-1-yl)-2-fluorobenzoic acid 
• 1443331-82-5 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)-2-fluoro-N-trideuteriomethylbenzamide 
• 1802242-43-8 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)-2-fluorobenzoic acid methyl ester 

Relevant articles and documents

METHOD FOR PREPARING DEUTERATED IMIDAZOLE DIKETONE COMPOUND

A method for preparation of deuterated imidazole diketone compounds includes the following steps: (1) using compound of formula (I) and compounds of formula (II) as starting material, compounds of formula (III) can be obtained by a substitution reaction; (2) Compounds of formula (IV) can be prepared by esterification of carboxyl in compounds of formula (III); (3) Cyclization of compounds of formula (IV) and compound of formula (V) provides compounds of formula (VI); (4) Compounds of formula (VI) are deesterificated and react to produce compounds of formula (VII); (5) using compounds of formula (VII) and compounds of formula (VIII) as starting material, the deuterated imidazole diketone compounds of formula (IX) are obtained by the condensation reaction of amide.

PROCESSES FOR THE SYNTHESIS OF DIARYLTHIOHYDANTOIN AND DIARYLHYDANTOIN COMPOUNDS

Processes are provided for the synthesis of diarylthiohydantoin and diarylhydantoin compounds, such as compounds of the formula: wherein X, Y1, Y2, R1, and R2 are as defined herein. Medicinal products containing the same find particular use in treating prostate cancer, including castration-resistant prostate cancer and/or hormone-sensitive prostate cancer.