14757-78-9

Basic information

• Product Name: 3-BROMO-2-FORMYLFURAN
• Synonyms: 3-BROMO-2-FORMYLFURAN;3-BROMO-FURAN-2-CARBALDEHYDE;3-Bromo-2-furaldehyde;3-Bromofuran-2-carboxaldehyde;3-Bromo-2-formylfuran, 3-Bromo-2-furaldehyde;3-Bromo-2-furaldehyde 98%;3-Bromo-2-formylfuran, 3-Bromofuran-2-carboxaldehyde;2-Furancarboxaldehyde, 3-broMo-
• CAS NO: 14757-78-9
• Molecular Formula: C₅H₃BrO₂
• Molecular Weight: 174.98
• Product Categories: Furan&Benzofuran;Furan;Halogenated;Organohalides
• Mol File: 14757-78-9.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 219.6±20.0℃ (760 Torr)
• Flash Point: 86.6±21.8℃
• Appearance: /
• Density: 1.748±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.118mmHg at 25°C
• Refractive Index: 1.573
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• CAS DataBase Reference: 3-BROMO-2-FORMYLFURAN(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-2-FORMYLFURAN(14757-78-9)
• EPA Substance Registry System: 3-BROMO-2-FORMYLFURAN(14757-78-9)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 22
• Hazardous Substances Data: 14757-78-9(Hazardous Substances Data)

Usage

Description

3-BROMO-2-FORMYLFURAN, also known as 3-Bromo-furan-2-carbaldehyde, is a chemical compound belonging to the class of furan derivatives. It is characterized by the presence of a bromine atom at the third position and a formyl group (aldehyde) at the second position in the furan ring structure. 3-BROMO-2-FORMYLFURAN is known for its potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
3-BROMO-2-FORMYLFURAN is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to serve as a building block in the development of new pharmaceutical compounds, contributing to the advancement of drug discovery and innovation.
Used in Chemical Synthesis:
3-BROMO-2-FORMYLFURAN is also used as a key intermediate in the synthesis of various organic compounds, particularly in the field of organic chemistry. Its reactivity and functional groups make it a valuable component in the creation of complex molecules and advanced materials.

InChI:InChI=1/C5H3BrO2/c6-4-1-2-8-5(4)3-7/h1-3H

Upstream product

• 22037-28-1 3-bromofurane 
• 4885-02-3 Dichloromethyl methyl ether 
• 38225-32-0 lithium isopropylamide 
• 68-12-2 N,N-dimethyl-formamide 
• 30544-34-4 2,3-dibromofuran 

Downstream Products

• 817186-42-8 3-phenylethynylfuran-2-carboxaldehyde 
• 1315568-11-6 6-phenylfuro[3,2-b]pyridin-5(4H)-one 
• 66488-00-4 3-benzylfuran-2-carbaldehyde 
• 35405-94-8 4H-Furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester 
• 1501968-64-4 ethyl 4-benzoyl-4H-furo[3,2-b]pyrrole-5-carboxylate 

Relevant articles and documents

π-Bridge Substitution in DASAs: The Subtle Equilibrium between Photochemical Improvements and Thermal Control**

Donor–acceptor Stenhouse adducts (DASAs) are playing an outstanding role as innovative and versatile photoswitches. Until now, all the efforts have been spent on modifying the donor and acceptor moieties to modulate the absorption energy and improve the c

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Preparation of amino-substituted indenes and 1,4-dihydronaphthalenes using a one-pot multireaction approach: Total synthesis of oxybenzo[c]phenanthridine alkaloids

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