1193-61-9

Basic information

• Product Name: 1-(1H-pyrrol-3-yl)propan-1-one
• CAS NO: 1193-61-9
• Molecular Formula: C₇H₉NO
• Molecular Weight: 123.1525
• Mol File: 1193-61-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 244.8°C at 760 mmHg
• Flash Point: 108.1°C
• Density: 1.063g/cm³
• Vapor Pressure: 0.0298mmHg at 25°C
• Refractive Index: 1.522
• CAS DataBase Reference: 1-(1H-pyrrol-3-yl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1H-pyrrol-3-yl)propan-1-one(1193-61-9)
• EPA Substance Registry System: 1-(1H-pyrrol-3-yl)propan-1-one(1193-61-9)

Safety Data

• Hazardous Substances Data: 1193-61-9(Hazardous Substances Data)

Usage

General Description

1-(1H-pyrrol-3-yl)propan-1-one, also known as 3-pyrrolylacetone, is an organic compound that belongs to the class of ketones. It is a colorless to light yellow liquid with a characteristic odor. 1-(1H-pyrrol-3-yl)propan-1-one is commonly used as a building block in the synthesis of pharmaceuticals and other organic compounds. It is also used in the production of fragrances and flavors. Additionally, 1-(1H-pyrrol-3-yl)propan-1-one has been studied for its potential pharmacological properties and has been found to exhibit antimicrobial and antioxidant activity. Overall, this compound has a diverse range of applications in the chemical, pharmaceutical, and flavor industries.

Upstream product

• 152171-06-7 1-[1-(toluene-4-sulfonyl)-1H-pyrrol-3-yl]propan-1-one 
• 109-97-7 pyrrole 
• 123-62-6 propionic acid anhydride 
• 79-03-8 propionyl chloride 

Downstream Products

• 111469-07-9 2-propyl-1,4-bis<(benzyloxycarbonyl)amino>butane 
• 99282-49-2 1-pyrrol-3-yl-propan-1-ol 
• 1551-09-3 3-Propylpyrrol 

Relevant articles and documents

An efficient and green method for regio- and chemo-selective Friedel-Crafts acylations using a deep eutectic solvent ([CholineCl][ZnCl2]3)

[CholineCl][ZnCl2]3, a deep eutectic solvent between choline chloride and ZnCl2, has been used as a dual function catalyst and green solvent for the Friedel-Crafts acylation of aromatic compounds instead of using the moisture-sensitive Lewis acids and volatile organic solvents. The reactions are performed with high yields under microwave irradiation with short reaction times for the synthesis of ketones. Interestingly, indole derivatives are regioselectively acylated in the 3-position under mild conditions with high yields without NH protection. Three new ketone products are synthesized. [CholineCl][ZnCl2]3 is easily synthesized from choline chloride and zinc chloride at a low cost, with easy purification and environmentally benign compounds. [CholineCl][ZnCl2]3 can be reused up to five times without loss of catalytic activity, making it ideal in industrial processes.