85553-51-1

Basic information

• Product Name: 2-(3-BROMOPHENYL)FURAN
• Synonyms: 2-(3-BROMOPHENYL)FURAN;3-BROMO-(2-FURYL)BENZENE;2-(3-Bromophenyl)furan 97%
• CAS NO: 85553-51-1
• Molecular Formula: C₁₀H₇BrO
• Molecular Weight: 223.07
• Mol File: 85553-51-1.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 266.829 °C at 760 mmHg
• Flash Point: 115.174 °C
• Appearance: /
• Density: 1.451 g/cm³
• Vapor Pressure: 0.014mmHg at 25°C
• Refractive Index: 1.576
• CAS DataBase Reference: 2-(3-BROMOPHENYL)FURAN(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-BROMOPHENYL)FURAN(85553-51-1)
• EPA Substance Registry System: 2-(3-BROMOPHENYL)FURAN(85553-51-1)

Safety Data

• Hazardous Substances Data: 85553-51-1(Hazardous Substances Data)

Usage

General Description

2-(3-Bromophenyl)furan is a chemical compound with the molecular formula C10H6BrO. It is a derivative of furan, a heterocyclic compound containing a five-membered ring with four carbon atoms and one oxygen atom. The presence of a bromine atom and a phenyl group in the compound's structure makes it useful in organic synthesis and medicinal chemistry. 2-(3-Bromophenyl)furan has potential applications in the development of pharmaceuticals, agrochemicals, and materials science. Its structure and properties make it a valuable building block for the synthesis of more complex molecules, and it may exhibit biological activity that could be useful in drug discovery and development.

InChI:InChI=1/C10H7BrO/c11-9-4-1-3-8(7-9)10-5-2-6-12-10/h1-7H

Upstream product

• 110-00-9 furan 
• 591-19-5 m-Bromoaniline 
• 591-18-4 1-Bromo-3-iodobenzene 
• 118486-94-5 2-(tributylstannyl)furan 
• 110-46-3 isopentyl nitrite 
• 3132-99-8 m-bromobenzoic aldehyde 
• 196953-06-7 1-(3-bromophenyl)-2,3-butadien-1-one 
• 89598-96-9 (3-bromophenyl)boronic acid 
• 27246-81-7 3-bromophenylhydrazine hydrochloride 

Downstream Products

• 85553-52-2 3-(furan-2-yl)benzaldehyde 
• 946647-07-0 C₄₉H₈₀N₂O₁₃ 
• 946647-06-9 C₄₉H₇₆N₂O₁₃ 
• 946647-05-8 C₄₉H₇₈N₂O₁₃ 

Relevant articles and documents

Black phosphorus as a metal-free, visible-light-active heterogeneous photoredox catalyst for the direct C-H arylation of heteroarenes

Black phosphorus (BP) is for the first time employed as a metal-free, heterogeneous photoredox catalyst for the direct C-H arylation of heteroarenes with aryl diazonium salts. The arylated heteroarenes are obtained in moderate to good yields under visible-light illumination, and the protocol is shown to be applicable for the scale-up synthesis.

Porphyrin-Catalyzed Photochemical C–H Arylation of Heteroarenes

Organic dyes are a promising class of photoredox catalysts and offer a meaningful alternative to broadly applied Ru and Ir complexes. We found that porphyrins with tuned physicochemical properties, by tailoring various substituents at the periphery of the

Gold(III) porphyrin-catalyzed cycloisomerization of allenones

Gold(III) porphyrin-catalyzed cycloisomerization of allenones gave the corresponding furans in good to excellent yields (up to 98%) and with quantitative substrate conversions. By recovering the Au(III) catalyst, a recyclable catalytic system is developed with over 8300 product turnovers attained for the cycloisomerization of 1-phenyl-buta-2,3-dien-1-one. The versatility of the gold(III) porphyrin catalyst was exemplified by its application to the hydroamination and hydration of phenylacetylene in 73% and 87% yield, respectively.