245762-35-0

Basic information

• Product Name: 5-Fluoro-2,3-dihydrobenzo[b]furan
• Synonyms: 5-FLUORO-2,3-DIHYDROBENZOFURAN;2,3-Dihydro-5-fluoroBenzo[B]furan;5-FLUORO-2,3-DIHYDROBENZO[B]FURAN;2,3-Dihydro-5-fluoro-1-benzofuran;5-Fluoro-2,3-dihydrobenzo[b...
• CAS NO: 245762-35-0
• Molecular Formula: C8H7FO
• Molecular Weight: 138.14
• EINECS: 246-331-6
• Mol File: 245762-35-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 191.559 °C at 760 mmHg
• Flash Point: 67.719 °C
• Appearance: /
• Density: 1.214 g/cm³
• Vapor Pressure: 0.711mmHg at 25°C
• Refractive Index: 1.535
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 5-Fluoro-2,3-dihydrobenzo[b]furan(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Fluoro-2,3-dihydrobenzo[b]furan(245762-35-0)
• EPA Substance Registry System: 5-Fluoro-2,3-dihydrobenzo[b]furan(245762-35-0)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 22
• Hazardous Substances Data: 245762-35-0(Hazardous Substances Data)

Usage

Physical Form

Liquid

Uses

5-Fluoro-2,3-dihydrobenzo[b]furan is a useful research chemical.

InChI:InChI=1/C8H7FO/c9-7-1-2-8-6(5-7)3-4-10-8/h1-2,5H,3-4H2

Upstream product

• 42933-43-7 2,3-dihydro-1-benzofuran-5-amine 
• 922728-20-9 2-bromo-1-(2-chloroethoxy)-4-fluorobenzene 
• 496-69-5 2-bromo-4-fluoro-phenol 
• 1572185-50-2 2-bromo-4-fluoro-6-methylphenol 
• 452-72-2 4-fluoro-2-methylphenol 
• 52059-53-7 2-(3-fluorophenyl)ethanol 
• 17403-47-3 5-nitro-2,3-dihydro-1-benzofuran 
• 496-16-2 2.3-dihydrobenzofuran 
• 59769-37-8 2-(4-Fluorophenoxy)-acetaldehyde Diethyl Acetal 
• 371-41-5 4-Fluorophenol 
• 24410-59-1 5-Fluoro[b]benzofuran 

Downstream Products

• 245762-37-2 5-fluoro-7-hydroxy-2,3-dihydrobenzofuran 
• 245762-36-1 5-fluoro-2,3-dihydrobenzofuran-7-carbaldehyde 

Relevant articles and documents

Compound for preparing PRC2 inhibitor, and preparation method and application thereof

The invention discloses a compound for preparing a PRC2 inhibitor, and a preparation method and application thereof. According to the method disclosed by the invention, a series of oximes can be simply and efficiently obtained, then a series of benzylamin

Synthesis of Functionalized Dihydrobenzofurans by Direct Aryl C?O Bond Formation under Mild Conditions

A method for the synthesis of dihydrobenzofurans by a direct aryl C?O bond formation is described. A mechanistic pathway for the reaction, distinct from previously described similar transformations, allows for mild reaction conditions that are expected to be compatible with functionalized substrates.

Nonsteroidal dissociated glucocorticoid agonists containing azaindoles as steroid A-ring mimetics

Syntheses and structure-activity relationships (SAR) of nonsteroidal glucocorticoid receptor (GR) agonists are described. These compounds contain azaindole moieties as A-ring mimetics and display various degrees of in vitro dissociation between gene trans