109812-64-8

Basic information

• Product Name: 2-METHYL-1,5-DIPHENYL-1H-PYRROLE-3-CARBOXYLIC ACID
• Synonyms: 1,5-DIPHENYL-2-METHYLPYRROLE-3-CARBOXYLIC ACID;2-METHYL-1,5-DIPHENYL-1H-PYRROLE-3-CARBOXYLIC ACID;BUTTPARK 97\57-04
• CAS NO: 109812-64-8
• Molecular Formula: C₁₈H₁₅NO₂
• Molecular Weight: 277.32
• Mol File: 109812-64-8.mol

Chemical Properties

• Melting Point: 226 °C
• Boiling Point: 487.5°Cat760mmHg
• Flash Point: 248.6°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 2.57E-10mmHg at 25°C
• Refractive Index: 1.606
• PKA: 5.56±0.50(Predicted)
• CAS DataBase Reference: 2-METHYL-1,5-DIPHENYL-1H-PYRROLE-3-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYL-1,5-DIPHENYL-1H-PYRROLE-3-CARBOXYLIC ACID(109812-64-8)
• EPA Substance Registry System: 2-METHYL-1,5-DIPHENYL-1H-PYRROLE-3-CARBOXYLIC ACID(109812-64-8)

Safety Data

• Hazard Codes: C
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 109812-64-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Applications:
2-Methyl-1,5-diphenyl-1H-pyrrole-3-carboxylic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, which includes a pyrrole core and phenyl substituents, may contribute to the development of new drugs with specific therapeutic properties.
Used in Material Science:
In the field of material science, 2-Methyl-1,5-diphenyl-1H-pyrrole-3-carboxylic acid is used as a building block for the creation of novel materials with tailored properties. The presence of the carboxylic acid group and the aromatic nature of the molecule may allow for the formation of new polymers or other materials with applications in various industries.
Used in Chemical Research:
2-Methyl-1,5-diphenyl-1H-pyrrole-3-carboxylic acid serves as a valuable compound for chemical research, particularly in the study of pyrrole chemistry and its potential applications. Researchers may use 2-METHYL-1,5-DIPHENYL-1H-PYRROLE-3-CARBOXYLIC ACID to explore new reaction pathways, investigate its reactivity, and understand its role in the synthesis of more complex molecules.

InChI:InChI=1/C18H15NO2/c1-13-16(18(20)21)12-17(14-8-4-2-5-9-14)19(13)15-10-6-3-7-11-15/h2-12H,1H3,(H,20,21)

Upstream product

• 109806-81-7 (2-methyl-1,5-diphenyl-pyrrol-3-yl)-glyoxal 
• 109693-68-7 (2-methyl-1,5-diphenyl-pyrrol-3-yl)-glyoxylonitrile 
• 3652-61-7 ethyl 2-methyl-1,5-diphenyl-1H-pyrrole-3-carboxylate 
• 52313-46-9 ethyl 2-acetyl-4-oxo-4-phenylbutanoate 
• 62-53-3 aniline 
• 52313-43-6 3-acetyl-1-phenyl-pentane-1,4-dione 
• 96757-78-7 1-(2-methyl-1,5-diphenyl-1H-pyrrol-3-yl)ethanone 
• 89201-10-5 α-Phenacyl-acetessigsaeure-aethylester 

Downstream Products

• 130850-59-8 4-Bromo-2-methyl-1,5-diphenyl-1H-pyrrole-3-carboxylic acid 

Relevant articles and documents

1,5-DIARYL-PYRROLE-3-CARBOXAMIDE DERIVATIVES AND THEIR USE AS CANNABINOID RECEPTOR MODULATORS

The present invention relates to a compound of formula (I) (A chemical formula should be inserted here - please see paper copy enclosed herewith) in which R1 and R2 independently represent phenyl, thienyl or pyridyl each of which is

AQUEOUS DISPERSION COMPRISING STABLE NANOPARTICLES OF A WATER-INSOLUBLE PYRROLE CARBOXAMIDE AND EXCIPIENT LIKE MIDDLE CHAIN TRIGLYCERIDES

A process for the preparation of a stable dispersion of solid particles, in an aqueous medium comprising combining (a) a first solution comprising a substantially water-insoluble substance which is a pyrrole carboxamide compound of Formula I, a water-misc

Oxidative Halogenation of Substituted Pyrroles with Cu(II). Part II. Bromination of some Ethyl 3-Pyrrolecarboxylates and Corresponding Acids

Ethyl 3-pyrrolecarboxylates and their corresponding acids are brominated with copper(II) bromide.The reaction afforded at 0 deg, with high-yield nuclear monobromination.