63762-78-7

Basic information

• Product Name: 2-FLUORO-5-METHYLANISOLE
• Synonyms: BUTTPARK 14\01-68;2-FLUORO-5-METHYLANISOLE;4-FLUORO-3-METHOXYTOLUENE;Fluoromethylanisole1;2-Fluoro-5-methylanisole, 97+%;2-Fluoro-5-methylanisole 98%;2-Fluoro-5-methylanisole98%;1-Fluoro-2-Methoxy-4-Methylbenzene
• CAS NO: 63762-78-7
• Molecular Formula: C₈H₉FO
• Molecular Weight: 140.15
• Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives;Aromatic Ethers;Ethers;Organic Building Blocks;Oxygen Compounds
• Mol File: 63762-78-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 176-177 °C(lit.)
• Flash Point: 174 °F
• Appearance: /
• Density: 1.070 g/mL at 25 °C(lit.)
• Vapor Pressure: 1.1mmHg at 25°C
• Refractive Index: n20/D 1.4950(lit.)
• BRN: 1862329
• CAS DataBase Reference: 2-FLUORO-5-METHYLANISOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FLUORO-5-METHYLANISOLE(63762-78-7)
• EPA Substance Registry System: 2-FLUORO-5-METHYLANISOLE(63762-78-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• RIDADR: 1993
• WGK Germany: 3
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 63762-78-7(Hazardous Substances Data)

Usage

General Description

2-Fluoro-5-methylanisole (FMA) undergoes" copolymerization" with other monomers and contains the nanoparticles, to form hydrogels useful for ophthalmic lenses.

InChI:InChI=1/C8H9FO/c1-6-3-4-7(9)8(5-6)10-2/h3-5H,1-2H3

Upstream product

• 39538-68-6 2-methoxy-4-methylaniline 
• 38512-82-2 3-methoxy-4-nitrotoluene 
• 452-84-6 3-amino-4-fluorotoluene 
• 63762-79-8 2-fluoro-5-methylphenol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 63762-81-2 1-fluoro-2-methoxy-4-methyl-5-nitrobenzene 
• 82846-18-2 4?fluoro-3-methoxybenzoic acid 
• 447463-95-8 2-fluoro-3-methoxy-5-methylbenzoic acid 
• 447462-92-2 2-fluoro-3-methoxy-5-methylphenol 
• 1452478-93-1 2-fluoro-1-methoxy-5-methyl-3-(methylsulfinyl)benzene 
• 1452478-94-2 2-fluoro-3-methoxy-5-methylbenzenethiol 
• 1452478-96-4 methyl 4-((2-fluoro-3-methoxy-5-methylphenyl)sulfanyl)-3-oxobutanoate 
• 550400-11-8 1-bromo-5-fluoro-4-methoxy-2-methylbenzene 
• 63762-80-1 2-nitro-4-fluoro-5-hydroxy-toluene 
• 63762-82-3 [(E)-2-(4-Fluoro-5-methoxy-2-nitro-phenyl)-vinyl]-dimethyl-amine 
• 128495-47-6 2-(4-fluoro-3-methoxyphenyl)nitroethylene 
• 128495-68-1 N-n-propyl-N-(2-phenylethyl)-2-(4-fluoro-3-hydroxyphenyl)ethylamine hydrobromide 
• 128495-66-9 N-ethyl-N-(2-phenylethyl)-2-(4-fluoro-3-hydroxyphenyl)ethylamine hydrobromide 
• 128495-67-0 N,N-di-n-propyl-2-(4-fluoro-3-hydroxyphenyl)ethylamine hydrobromide 

Relevant articles and documents

Synthesis and Dopamine Receptor Affinities of 2-(4-fluoro-3-hydroxyphenyl)ethylamine and N-Substituted Derivatives

The synthesis of 2-(4-fluoro-3-hydroxyphenyl)ethylamine (26) and of some N,N-dialkyl derivatives (27-30) starting from 4-fluoro-3-hydroxytoluene and their in vitro binding affinities for dopamine (DA) receptor are reported.The amine 26 can be regarded as

Synthesis and evaluation of the antiovulatory activity of a variety of melatonin analogues

A series of melatonin analogues was synthesized and examined for ovulation-blocking activity. Deviation from the 5-methoxy group or substitution of the 1 position prevented activity. Activity was not particularly sensitive to minor variations in the N-acyl group nor was it significantly altered by methylation of position 2 or the α-methylene; however, a pronounced enhancement resulted from halogenation of the 6 position.