341-41-3

Basic information

• Product Name: 1-BROMO-4-FLUORONAPHTHALENE
• Synonyms: BUTTPARK 44\09-75;1-FLUORO-4-BROMONAPHTHALENE;1-BROMO-4-FLUORONAPHTHALENE;1-Bromo-4-fluoronaphthalene,98%;1-Bromo-4-fluoronaphthalene 98%;1-Bromo-4-fluonaphthalene
• CAS NO: 341-41-3
• Molecular Formula: C₁₀H₆BrF
• Molecular Weight: 225.06
• EINECS: 206-434-9
• Product Categories: Naphthalene derivatives;Aryl;C9 to C12;Halogenated Hydrocarbons
• Mol File: 341-41-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 35-38 °C(lit.)
• Boiling Point: 281.4°Cat760mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.563g/cm³
• Vapor Pressure: 0.00609mmHg at 25°C
• Refractive Index: 1.638
• Storage Temp.: 0-10°C
• Solubility: Chloroform (Slightly), DMSO (Slightly)
• BRN: 2085804
• CAS DataBase Reference: 1-BROMO-4-FLUORONAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-4-FLUORONAPHTHALENE(341-41-3)
• EPA Substance Registry System: 1-BROMO-4-FLUORONAPHTHALENE(341-41-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 341-41-3(Hazardous Substances Data)

Usage

Chemical Properties

Solid

Uses

1-Bromo-4-fluoronaphthalene is the starting material for the synthesis of Fluorobenzo[c]fluoren (F588435) which is a polycyclic aromatic hydrocarbon used in materials science extensively due to utility in organic electronics, light emitting diodes and solar cells.

InChI:InChI=1/C10H6BrF/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H

Upstream product

• 321-38-0 1-Fluoronaphthalene 
• 56-23-5 tetrachloromethane 
• 7726-95-6 bromine 

Downstream Products

• 3870-18-6 2-(4-fluoro-[1]naphthoyl)-benzoic acid 
• 1536-34-1 p-Tolyl-<4-fluor-naphthyl-(1)>-keton 
• 1536-33-0 m-Tolyl-<4-fluor-naphthyl-(1)>-keton 
• 1827-58-3 2-(4-fluoronaphthalen-1-yl)cyclohexan-1-one 
• 17318-09-1 1-iodo-4-fluoronaphthalene 
• 1536-17-0 1-Carboxymethyl-2-<4-fluor-naphthyl-(1)>-cyclohexanol-(1) 
• 182344-25-8 (4-fluoronaphthalen-1-yl)boronic acid 
• 151983-15-2 trans 1-(4-fluoro-1-naphthalenyl)-4-[4-(phenylmethyl)-1-piperazinyl]cyclohexanol 
• 38659-72-2 (C₆H₅)3SnCH₂C₁₀H₆F 
• 1232143-74-6 tert-butyl 4-{(1R)-1-[(4-fluoro-1-naphthyl)(hydroxy)(4-methoxyphenyl)methyl]butyl}benzoate 
• 627526-35-6 2-(4-fluoronaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant articles and documents

4-fluoronaphthalene-1-alcohol preparation technology

The invention discloses a 4-fluoronaphthalene-1-alcohol preparation technology. The preparation technology takes 1-fluoronaphthalene as a raw material, the raw material is subjected to halogenation, boration and hydrolysis to obtain the 4-fluoronaphthalene-1-alcohol, and the overall yield can reach 60%. The technology has the advantages of low cost and easy acquisition of the raw materials, simple and easy operation of post-treatment t, high yield, and easy industrial application.

2-aminopyridines containing fused ring substituents

The present invention relates to 2-aminopyridine derivatives of the formula wherein G, R1 and R2 are defined as in the specification, that exhibit activity as nitric oxide synthase (NOS) inhibitors, to pharmaceutical compositions containing them and to their use in the treatment and prevention of central nervous system and other disorders.