70375-79-0

Basic information

• Product Name: METHYL 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBOXYLATE
• Synonyms: METHYL 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBOXYLATE;1H-Pyrazole-3-carboxylic acid, 1,5-diphenyl-, Methyl ester
• CAS NO: 70375-79-0
• Molecular Formula: C₁₇H₁₄N₂O₂
• Molecular Weight: 278.31
• Mol File: 70375-79-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 453.1°C at 760 mmHg
• Flash Point: 227.9°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 2.12E-08mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: METHYL 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBOXYLATE(70375-79-0)
• EPA Substance Registry System: METHYL 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBOXYLATE(70375-79-0)

Safety Data

• Hazardous Substances Data: 70375-79-0(Hazardous Substances Data)

Usage

General Description

Methyl 1,5-diphenyl-1H-pyrazole-3-carboxylate is a chemical compound with the molecular formula C19H16N2O2. It is a pyrazole derivative that is commonly used in organic synthesis and medicinal chemistry research. METHYL 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBOXYLATE is characterized by its aromatic, heterocyclic structure and is often utilized as a building block in the synthesis of various pharmaceuticals and organic compounds. The carboxylate group in its structure makes it a versatile molecule that can participate in a wide range of chemical reactions, and it has demonstrated potential as a pharmacologically active compound in some studies. Overall, methyl 1,5-diphenyl-1H-pyrazole-3-carboxylate is a valuable and versatile chemical with applications in both research and industrial settings.

InChI:InChI=1/C17H14N2O2/c1-21-17(20)15-12-16(13-8-4-2-5-9-13)19(18-15)14-10-6-3-7-11-14/h2-12H,1H3

Upstream product

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Downstream Products

• 13599-22-9 1,5-diphenylpyrazole-3-carboxylic acid 
• 945984-78-1 (1,5-diphenyl-1H-pyrazol-3-yl)-methanol 
• 176230-62-9 4-chloro-1,5-diphenyl-1H-pyrazole-3-carboxylic acid methyl ester 

Relevant articles and documents

Design, syntheses and antitumor activities evaluation of 1,5-diaryl substituted pyrazole secnidazole ester derivatives

According to the drug hybridization principle, a series of novel 1,5-diaryl substituted pyrazole secnidazole ester derivatives (6aa–6gc) have been synthesized by the combinations of various 1,5-diarylpyrazole-3-carboxylic acids with secnidazole. The in vi

Design and biological evaluation of novel hybrids of 1, 5-diarylpyrazole and Chrysin for selective COX-2 inhibition

The overexpress of COX-2 was clearly associated with carcinogenesis and COX-2 as a possible target has long been exploited for cancer therapy. In this work, we described the design and synthesis of a series of diarylpyrazole derivatives integrating with c

When aryldiazonium salts meet vinyl diazoacetates: A cobalt-catalyzed regiospecific synthesis of N-arylpyrazoles

A cobalt-catalyzed C-N bond formation between aryl diazonium salts and vinyl diazoacetates has been developed under relatively mild conditions. The N-arylpyrazoles have been prepared in moderate to high yields in a regiospecific way.