27363-77-5 Usage
Description
2-(3,5-DIMETHYL-PYRAZOL-1-YL)-BENZOIC ACID is a chemical compound with the molecular formula C12H12N2O2, characterized by its benzoic acid structure and a pyrazole ring. This derivative is known for its potential applications in medicinal chemistry, particularly in the synthesis of pharmaceutical agents.
Uses
Used in Pharmaceutical Industry:
2-(3,5-DIMETHYL-PYRAZOL-1-YL)-BENZOIC ACID is used as a key intermediate in the synthesis of various pharmaceutical agents due to its unique structure and properties. It plays a crucial role in the development of new drugs with potential therapeutic benefits.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-(3,5-DIMETHYL-PYRAZOL-1-YL)-BENZOIC ACID is used as a promising candidate for research and development. Its antimicrobial and anti-inflammatory properties make it a valuable compound for exploring new treatment options and advancing pharmaceutical formulations.
Used in Antimicrobial Applications:
2-(3,5-DIMETHYL-PYRAZOL-1-YL)-BENZOIC ACID is employed as an antimicrobial agent, demonstrating effectiveness against various microorganisms. Its ability to inhibit microbial growth makes it a potential candidate for use in treatments targeting infectious diseases.
Used in Anti-inflammatory Applications:
2-(3,5-DIMETHYL-PYRAZOL-1-YL)-BENZOIC ACID is also used as an anti-inflammatory agent, showing potential in reducing inflammation and associated symptoms. This property makes it a candidate for further research in the development of anti-inflammatory medications.
Check Digit Verification of cas no
The CAS Registry Mumber 27363-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,6 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27363-77:
(7*2)+(6*7)+(5*3)+(4*6)+(3*3)+(2*7)+(1*7)=125
125 % 10 = 5
So 27363-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c1-8-7-9(2)14(13-8)11-6-4-3-5-10(11)12(15)16/h3-7H,1-2H3,(H,15,16)
27363-77-5Relevant articles and documents
Ruthenium-catalyzed c-h silylation of 1-arylpyrazole derivatives and fluoride-mediated carboxylation: Use of two nitrogen atoms of the pyrazole Group
Mita, Tsuyoshi,Tanaka, Hiroyuki,Michigami, Kenichi,Sato, Yoshihiro
supporting information, p. 1291 - 1294 (2014/06/10)
Carboxylation of 1-arylpyrazole derivatives was developed using a ruthenium-catalyzed ortho silylation in conjunction with fluoride-mediated carboxylation with carbon dioxide. The two nitrogen atoms of pyrazole play crucial roles in promoting ortho silylation via the formation of a five-membered ruthenacycle and in accelerating aryl anion formation by lowering the electron density of the aromatic ring. Georg Thieme Verlag Stuttgart New York.
