73799-68-5

Basic information

• Product Name: 1H-Pyrrole-3-carboxylicacid,4,5-diphenyl-,ethylester(9CI)
• Synonyms: 1H-Pyrrole-3-carboxylicacid,4,5-diphenyl-,ethylester(9CI)
• CAS NO: 73799-68-5
• Molecular Formula: C₁₉H₁₇NO₂
• Molecular Weight: 291.34
• Product Categories: HANTZSCH
• Mol File: 73799-68-5.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrole-3-carboxylicacid,4,5-diphenyl-,ethylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-3-carboxylicacid,4,5-diphenyl-,ethylester(9CI)(73799-68-5)
• EPA Substance Registry System: 1H-Pyrrole-3-carboxylicacid,4,5-diphenyl-,ethylester(9CI)(73799-68-5)

Safety Data

• Hazardous Substances Data: 73799-68-5(Hazardous Substances Data)

Usage

Heterocyclic compound

A compound with a five-membered ring containing four carbon atoms and one nitrogen atom This describes the structure of the 1H-pyrrole-3-carboxylic acid core in the molecule.

Ethyl ester derivative

A derivative of 1H-pyrrole-3-carboxylic acid with an ethyl ester group This indicates that the compound is derived from 1H-pyrrole-3-carboxylic acid by attaching an ethyl ester group to it.

Presence of phenyl groups

The molecule contains two phenyl groups (C6H5) This contributes to the compound's aromaticity and may influence its chemical properties and potential applications.

Highly aromatic compound

The presence of phenyl groups makes the compound highly aromatic This means that the compound has a strong aroma and a stable, delocalized electron system across the aromatic rings.

Potential applications

Pharmaceutical, agrochemical, and materials science Due to its unique chemical structure and properties, the compound may have various applications in these fields.

Limited information

Detailed information about specific uses and potential hazards is limited This highlights the need for further research and testing to fully understand the compound's potential applications and safety considerations.

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Relevant articles and documents

Selective synthesis of trisubstituted pyrroles through the reactions of alkynyl Fischer carbene complexes with oxazolones

An efficient and simple synthesis of novel trisubstituted 1H-pyrroles 4a-qvia 1,3-dipolar cycloaddition of Δ3-trifluoromethyloxazolones 2a-d with both chromium and tungsten alkynyl Fischer carbene complexes (1a-h) is described. An unexpected and unreported -CF3 group elimination process was observed in the pyrrole structure. Our experimental and theoretical data suggested that the metal fragment may be responsible for this phenomenon. The dipolar cycloaddition proceeded efficiently to produce a single regioisomer, which was unambiguously established through NMR and single-crystal X-ray diffraction studies. Nevertheless, the reaction of alkynyl carbenes bearing an α,β,γ,δ-unsaturated moiety with excess oxazolone 2a produced a polycyclic compound 6 speculatively formed through a cascade reaction involving 1,6-, 1,4- and 1,2-nucleophilic addition steps.

Synthesis of substituted pyrroles from N-vinylic phosphazenes derived from β-amino acids and α-bromo ketones

Synthesis of di-, tri- and tetrasubstituted pyrroles by reaction of Nvinylic phosphazenes derived from β-amino acids with α-bromo ketones is described.

Antiinflammatory 4,5-diaryl-α-polyfluoroalkyl-1H-pyrrole-2-methanols and method for use thereof

4,5-Diaryl-α-polyfluoroalkyl-1H-pyrrole-2-methanols, such as 4,5-bis (4-fluorophenyl)-α, α-bis (trifluoromethyl)-1H-pyrrole-2-methanol, are useful in treatment of inflammation and relieving pain.