79852-26-9

Basic information

• Product Name: 1-(5-METHYLTHIEN-2-YL)BUTAN-1-ONE
• Synonyms: 1-(5-METHYLTHIEN-2-YL)BUTAN-1-ONE;Nsc80376;1-(5-methyl-2-thienyl)butan-1-one(SALTDATA: FREE)
• CAS NO: 79852-26-9
• Molecular Formula: C₉H₁₂OS
• Molecular Weight: 168.26
• Mol File: 79852-26-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 267.6°C at 760 mmHg
• Flash Point: 115.6°C
• Appearance: /
• Density: 1.053g/cm³
• Vapor Pressure: 0.00809mmHg at 25°C
• Refractive Index: 1.522
• CAS DataBase Reference: 1-(5-METHYLTHIEN-2-YL)BUTAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5-METHYLTHIEN-2-YL)BUTAN-1-ONE(79852-26-9)
• EPA Substance Registry System: 1-(5-METHYLTHIEN-2-YL)BUTAN-1-ONE(79852-26-9)

Safety Data

• Hazardous Substances Data: 79852-26-9(Hazardous Substances Data)

Usage

General Description

1-(5-Methylthien-2-yl)butan-1-one is a chemical compound with the molecular formula C9H12OS. It is an organic compound containing a thienyl group, which is a five-membered heterocyclic ring containing sulfur. The compound is a ketone, with the thienyl group attached to the first carbon of a butanone chain. This chemical may have various industrial applications, including use as a building block in the synthesis of other organic compounds. It is also important to handle this chemical with care as it may have some risks and hazards associated with its use. Overall, 1-(5-Methylthien-2-yl)butan-1-one is a versatile compound with potential applications in various industries.

InChI:InChI=1/C9H12OS/c1-3-4-8(10)9-6-5-7(2)11-9/h5-6H,3-4H2,1-2H3

Upstream product

• 554-14-3 2-Methylthiophene 
• 106-31-0 butanoic acid anhydride 
• 141-75-3 butyryl chloride 
• 879981-00-7 1-(5-methylthiophen-2-yl)butan-1-ol 

Downstream Products

• 1918-79-2 2-methylthiophene-5-carboxylic acid 
• 79852-37-2 1-(2-Benzyl-5-methyl-2,5-dihydro-thiophen-2-yl)-butan-1-one 
• 79852-45-2 C₁₆H₂₀O 
• 79852-41-8 1-(2-Benzyl-5-methyl-1,1-dioxo-2,5-dihydro-1H-1λ⁶-thiophen-2-yl)-butan-1-one 

Relevant articles and documents

Iodine promoted α-hydroxylation of ketones

A novel method for α-hydroxylation of ketones using substoichiometric amount of iodine under metal-free conditions is described. This method has been successfully employed in synthesizing a variety of heterocyclic compounds, which are useful precursors. α-Hydroxylation of diketones and triketones are illustrated. This strategy provides a novel, efficient, mild and inexpensive method for α-hydroxylation of aryl ketones using a sub-stoichiometric amount of molecular iodine.

A new and highly efficient water-soluble copper complex for the oxidation of secondary 1-heteroaryl alcohols by tert-butyl hydroperoxide

The water-soluble copper complex generated in situ from CuCl2 and 2,2′-biquinoline-4,4′-dicarboxylic acid dipotassium salt (BQC), has been revealed as a highly efficient and selective catalyst for the oxidation of secondary 1-heteroaryl alcohols to the corresponding heteroaromatic ketones with aqueous tert-butyl hydroperoxide, under mild conditions. The catalytic system is compatible with different heterocycles such as pyridines, pyrroles, indoles, thiophens, furans, thiazoles, and imidazoles.