77169-12-1 Usage
Description
1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is a pyrazole derivative with the molecular formula C17H13N3O2, belonging to the class of carboxylic acids. This chemical compound possesses a unique structure that endows it with potential applications in various fields, including medicinal chemistry, agrochemicals, and other industrial uses. Its biological properties also make it a promising candidate for further research and development in therapeutic or diagnostic applications.
Uses
Used in Medicinal Chemistry:
1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used as a starting material for the synthesis of pharmaceuticals, owing to its unique chemical structure and potential biological properties. It can be utilized in the development of new drugs with specific therapeutic effects.
Used in Agrochemicals Production:
1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used in the production of agrochemicals, where its chemical properties can be harnessed to create effective compounds for agricultural applications, such as pesticides or herbicides.
Used in Other Industrial Applications:
1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID may have uses in various industrial applications, where its unique chemical structure and properties can be employed to develop new materials or improve existing ones.
Used in Research and Development:
1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is used in research and development for potential therapeutic or diagnostic purposes, as its biological properties may offer new avenues for the treatment or detection of diseases. Further studies are required to explore its full potential in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 77169-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77169-12:
(7*7)+(6*7)+(5*1)+(4*6)+(3*9)+(2*1)+(1*2)=151
151 % 10 = 1
So 77169-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H12N2O2/c19-16(20)14-11-18(13-9-5-2-6-10-13)17-15(14)12-7-3-1-4-8-12/h1-11H,(H,19,20)/p-1
77169-12-1Relevant articles and documents
Urea derivatives of piperazine doped with pyrazole-4-carboxylic acids: Synthesis and antimicrobial evaluation
Devi, Vandana,Phougat, Harshita,Rai, Sanjay,Reddy, T. Shreedhar,Singh, Karan
, (2021/07/06)
A series of novel N-cycloalkyl/aryl-4-(1,3-diphenyl-1H-pyrazole-4-carbonyl)piperazine-1-carboxamides 9a-g has been synthesized for biological interest by simple base catalyzed reaction of various N-cycloalkyl/aryl isocyanates with (1,3-diphenyl-1H-pyrazol
Novel carboxamide compound and compositions for preventing or treating metabolic diseases comprising the same
-
, (2021/09/14)
The present invention relates to a novel carboxamide compound and a composition for preventing or treating metabolic diseases comprising the same, wherein the composition is potent and selective estrogen related receptor (Estrogen-related receptor). ERR)
Pyrazole-4-carboxylic Acids from Vanadium-catalyzed Chemical Transformation of Pyrazole-4-carbaldehydes
Bala, Renu,Kumari, Poonam,Sood, Sumit,Phougat, Harshita,Kumar, Anil,Singh, Karan
, p. 1787 - 1793 (2019/04/30)
The conversion of aldehydes into carboxylic acids using oxidizing agents is a common protocol in transformation chemistry. An efficient oxidation strategy of transformation of pyrazole-4-aldehydes to the corresponding acids using vanadium catalysts in the presence of 30% H2O2 as an oxidant is described. The catalytic technology was successfully applied to a range of various 4-formylpyrazoles, and plausible mechanism is also discussed.
