699-22-9

Basic information

• Product Name: 1-Pentyl-1H-pyrrole
• Synonyms: 1-Pentyl-1H-pyrrole
• CAS NO: 699-22-9
• Molecular Formula: C₉H₁₅N
• Molecular Weight: 137.22
• Mol File: 699-22-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Pentyl-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pentyl-1H-pyrrole(699-22-9)
• EPA Substance Registry System: 1-Pentyl-1H-pyrrole(699-22-9)

Safety Data

• Hazardous Substances Data: 699-22-9(Hazardous Substances Data)

Usage

Chemical class

Pyrrole

Structure

Five-membered aromatic ring containing one nitrogen atom

Usage

Synthesis of various materials and compounds, potential pharmaceutical applications, precursor for the synthesis of semiconducting materials, potential use as a flavoring agent in the food industry

Interest

Diverse range of applications, of interest in various fields of scientific research.

Upstream product

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Relevant articles and documents

Nickel-Catalyzed Synthesis of N-Substituted Pyrroles Using Diols with Aryl- and Alkylamines

Herein, nickel-catalyzed sustainable strategy for the synthesis of N-substituted pyrroles using butene-1,4-diols and butyne-1,4-diols with a series of aryl-, alkyl-, and heteroarylamines is reported. The catalytic protocol is tolerant of free alcohol, halide, alkyl, alkoxy, oxygen heterocycles, activated benzyl, and the pyridine moiety and resulted in up to 90% yield. Initial mechanistic studies involving defined nickel catalyst, determination of rate, and order of reaction including deuterium-labeling experiments were performed for pyrrole synthesis.

Remarkable fast n-alkylation of azaheterocycles under microwave irradiation in dry media

Under microwave irradiation a number of azaheterocycles (i.e., pyrrole, imidazole, pyrazole, indole, and carbazole) react remarkably fast with alkyl halides to give exclusively N-alkyl derivatives.