1634-53-3

Basic information

• Product Name: 2-Bromo-1-(5-methylfuran-2-yl)-ethanone
• Synonyms: 2-Bromo-1-(5-methylfuran-2-yl)-ethanone
• CAS NO: 1634-53-3
• Molecular Formula: C₇H₇BrO₂
• Molecular Weight: 203.04
• Mol File: 1634-53-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Bromo-1-(5-methylfuran-2-yl)-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-1-(5-methylfuran-2-yl)-ethanone(1634-53-3)
• EPA Substance Registry System: 2-Bromo-1-(5-methylfuran-2-yl)-ethanone(1634-53-3)

Safety Data

• Hazardous Substances Data: 1634-53-3(Hazardous Substances Data)

Usage

General Description

2-Bromo-1-(5-methylfuran-2-yl)-ethanone is a chemical compound with the molecular formula C8H7BrO2. It is a derivative of furan, a five-membered aromatic ring with one oxygen atom, and it contains a bromine and a ketone functional group. 2-Bromo-1-(5-methylfuran-2-yl)-ethanone is commonly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It has been identified as a potential building block for the synthesis of various bioactive molecules. Additionally, it has been studied for its potential use as a reagent in the development of new chemical reactions and transformations. However, it is important to handle this compound with care, as it may have potential health hazards and should be used in a controlled laboratory setting.

Upstream product

• 1193-79-9 2-acetyl-5-methylfuran 

Downstream Products

• 1634-46-4 4-(5-methylfuran-2-yl)thiazol-2-amine 

Relevant articles and documents

Bromination of 2-acetyl-5-methylfuran

The bromination of 2-acetyl-5-methylfuran by bromine and N-bromosuccinimide was studied. The action of N-bromosuccinimide on 5-methyl-2-acetylfuran in various solvents leads to mixtures of an ω-bromo ketone, a 5-bromomethyl derivative, and 5-bromomethyl-ω-bromo ketone. The use of 2,2′-azobisisobutyronitrile as activator of the radical process does not make the reaction selective but promotes bromination at the methyl group of the ring. A selective method for the synthesis of 2-(bromoacetyl)-5-methylfuran by the bromination of 2-acetyl-5-methylfuran with bromine was developed. 1999 KluwerAcademic/Plenum.

UREA DERIVATIVES METHODS FOR THEIR MANUFACTURE AND USES THEREOF

The present invention provides compounds of formula (I): in which R 1, R'1, R2, R'2, R3, Y and G have the meanings given in the description, to a process for their preparation, their application by way of medicaments, and to pharmaceutical compositions containing them.

Pyridoquinoxaline antivirals

The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof wherein R1, R2 and R3 are as defined in the specification. The compounds are useful for the treatment of viral infections.