22186-60-3

Basic information

• Product Name: 2-(1H-pyrrol-2-yl)ethanol
• Synonyms: 2-(1H-pyrrol-2-yl)ethanol
• CAS NO: 22186-60-3
• Molecular Formula: C₆H₉NO
• Molecular Weight: 111.14176
• Mol File: 22186-60-3.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 245.3°Cat760mmHg
• Flash Point: 102.2°C
• Appearance: /
• Density: 1.133g/cm³
• Vapor Pressure: 0.0154mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: 2-(1H-pyrrol-2-yl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1H-pyrrol-2-yl)ethanol(22186-60-3)
• EPA Substance Registry System: 2-(1H-pyrrol-2-yl)ethanol(22186-60-3)

Safety Data

• Hazardous Substances Data: 22186-60-3(Hazardous Substances Data)

Usage

General Description

2-(1H-pyrrol-2-yl)ethanol, also known as pyrrole-2-ethanol, is a chemical compound with the molecular formula C6H9NO. It is a colorless to yellowish liquid that is commonly used in the synthesis of pharmaceuticals and agrochemicals. Pyrrole-2-ethanol has been found to exhibit antibacterial and antifungal properties, making it a potential candidate for use in antimicrobial formulations. Additionally, it has been studied for its potential as a chelating agent for metal ions and as a building block in organic synthesis. Overall, 2-(1H-pyrrol-2-yl)ethanol is a versatile compound with a range of potential applications in various industries.

InChI:InChI=1/C6H9NO/c8-5-3-6-2-1-4-7-6/h1-2,4,7-8H,3,5H2

Upstream product

• 53912-79-1 pyrrol-2-yl-acetic acid methyl ester 
• 3768-70-5 Pyrryl-2-glyoxylylchlorid 
• 75-21-8 oxirane 
• 96999-22-3 n-octyl pyrrole-2-glyoxalate 
• 109-97-7 pyrrole 
• 4778-25-0 (1H-pyrrol-2-yl)acetic acid ethyl ester 

Downstream Products

• 1551-06-0 2-ethyl-1H-pyrrole 
• 84573-35-3 perhydropyrrolo<1,2-c><1,3>oxazine 
• 175689-47-1 <1-(1,1-dimethylethoxycarbonyl)-2-pyrrolyl>ethyl 2-diazo-4-phenyl-3(E)-butenoate 
• 175689-46-0 2-(2-pyrrolyl)ethyl 4-phenyl-3(E)-butenoate 
• 19432-88-3 2-(β-hydroxyethyl)-pyrrolidine 

Relevant articles and documents

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Novel quinazoline derivative LU1502 as well as preparation method and application thereof

The invention discloses a novel quinazoline derivative LU1502 as well as a preparation method thereof. The quinazoline derivative LU1502 is chemically named N-[(4-fluorophenyl)methyl]-4-N-[7-methoxy-6-[2-(1-pyrrole-2-yl)hydroxyethyl]quinazoline-4-yl]-1,4-diamine. The quinazoline derivative as well as pharmaceutically acceptable salts, solvates and hydrates thereof has excellent in-vitro and in-vivo anti-tumor activity for MDA-MB-435, SK-BR-3, A549, HCT 115 and MDA-MB-468 and has brighter application prospect in preparation of anti-tumor drugs.

Novel quinazoline derivative LU1510 as well as preparation method and application thereof

The invention discloses a novel quinazoline derivative LU1510 as well as a preparation method thereof. The quinazoline derivative LU1510 is chemically named N-4-[(4-dimethylamino phenyl)methoxy]phenyl-7-methoxy-6-[(1-pyrrole-2-yl)hydroxyethyl]quinazoline-