77169-12-1

Basic information

• Product Name: 1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
• Synonyms: VITAS-BB TBB000124;1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID;AKOS B006503;BUTTPARK 145\04-52;ART-CHEM-BB B006503;1,3-diphenylpyrazole-4-carboxylic acid
• CAS NO: 77169-12-1
• Molecular Formula: C₁₆H₁₂N₂O₂
• Molecular Weight: 264.28
• Mol File: 77169-12-1.mol
• Article Data: 20

Chemical Properties

• Boiling Point: 451.4°C at 760 mmHg
• Flash Point: 226.8°C
• Appearance: /
• Vapor Pressure: 6.17E-09mmHg at 25°C
• CAS DataBase Reference: 1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID(77169-12-1)
• EPA Substance Registry System: 1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID(77169-12-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• HazardClass: IRRITANT
• Hazardous Substances Data: 77169-12-1(Hazardous Substances Data)

Usage

General Description

1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID is a chemical compound with the molecular formula C17H13N3O2. It is a pyrazole derivative and belongs to the class of carboxylic acids. 1,3-DIPHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID has various potential applications, including in the field of medicinal chemistry as a starting material for the synthesis of pharmaceuticals. It may also have uses in the production of agrochemicals or other industrial applications. Additionally, it may have biological properties that could make it suitable for further research and development for potential therapeutic or diagnostic purposes.

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

Upstream product

• 55849-26-8 (α-nitrobenzylidene)phenylhydrazine 
• 922-67-8 propynoic acid methyl ester 
• 21487-45-6 1,3-diphenyl-4-formylpyrazole 
• 583-11-9 N-(1-phenylethylidene)phenylhydrazine 
• 98-86-2 acetophenone 
• 100-63-0 phenylhydrazine 
• 59-88-1 phenylhydrazine hydrochloride 

Downstream Products

• 4492-01-7 1,3-diphenyl-1H-pyrazole 
• 443912-26-3 1,3-diphenyl-1H-pyrazole-4-carbonyl azide 
• 443912-31-0 4-isocyanato-1,3-diphenyl-1H-pyrazole 
• 125103-40-4 1,3-Diphenyl-1H-pyrazole-4-carboxylic acid amide 
• 125103-41-5 (4-Benzyl-piperazin-1-yl)-(1,3-diphenyl-1H-pyrazol-4-yl)-methanone; hydrochloride 
• 917947-75-2 2-(1,3-diphenyl-1H-pyrazol-4-yl)-5-phenyl-1,3,4-oxadiazole 

Relevant articles and documents

Urea derivatives of piperazine doped with pyrazole-4-carboxylic acids: Synthesis and antimicrobial evaluation

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

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

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.