19336-75-5 Usage
Description
2-[[(2-FLUOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is a chemical compound with the molecular formula C12H9FNO3. It is a derivative of benzoic acid, featuring a carboxylic acid group, a fluorophenyl group, and an amino carbonyl group. 2-[[(2-FLUOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is widely used in organic synthesis and pharmaceutical research due to its potential medicinal properties, including anti-inflammatory and analgesic effects, making it a promising target for drug development. Its unique structure also suggests that it may possess other biological activities, such as binding to specific receptors.
Uses
Used in Pharmaceutical Industry:
2-[[(2-FLUOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is used as a pharmaceutical intermediate for the development of new drugs. Its anti-inflammatory and analgesic properties make it a potential candidate for the treatment of various inflammatory and pain-related conditions.
Used in Organic Synthesis:
2-[[(2-FLUOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is used as a key building block in the synthesis of various organic compounds. Its unique structure allows for the formation of diverse chemical entities with potential applications in various fields.
Used in Medicinal Chemistry Research:
2-[[(2-FLUOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is used as a research tool in medicinal chemistry to explore its potential as a lead compound for the development of new therapeutic agents. Its ability to bind to specific receptors and exhibit biological activities makes it an interesting subject for further investigation.
Used in Drug Discovery:
2-[[(2-FLUOROPHENYL)AMINO]CARBONYL]-BENZOIC ACID is used in drug discovery processes to identify novel therapeutic targets and develop new drugs with improved efficacy and safety profiles. Its potential medicinal properties and unique structure make it a valuable asset in the search for innovative treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 19336-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,3 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19336-75:
(7*1)+(6*9)+(5*3)+(4*3)+(3*6)+(2*7)+(1*5)=125
125 % 10 = 5
So 19336-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H10FNO3/c15-11-7-3-4-8-12(11)16-13(17)9-5-1-2-6-10(9)14(18)19/h1-8H,(H,16,17)(H,18,19)
19336-75-5Relevant articles and documents
Microwave assisted synthesis of N-Arylphthalamic acids with hyperlipidemic activity
Sena, Vera L.M,Srivastava, Rajendra M,Oliveira, Shalom P,Lima, Vera L.M
, p. 2671 - 2674 (2001)
A series of substituted N-arylphthalamic acids 3a-i has been synthesized by the reaction of phthalic anhydride 1 and aryl- or heterocyclic amines 2a-i, in the absence of solvents, in a domestic microwave oven. The formation of nine N-arylphthalamic acids was accomplished in 1-3 min giving excellent yields for compounds 3a-g, but moderate yield of compounds 3h and 3i, respectively. Compounds 3h and 3i are new. Interestingly, N-arylphthalamic acids 3a-i induced hyperlipidemia in Swiss white mice and also increased animals' body weight.
