104197-14-0

Basic information

• Product Name: 4-Bromo-2,6-difluoroanisole
• Synonyms: 4-BROMO-2,6-DIFLUOROANISOLE;4-Bromo-2,6-difluoroanisole, 97+%;4-Bromo-2,6-difluoroanisole 98%;4-Bromo-2,6-difluoroanisole98%;5-bromo-1,3-difluoro-2-methoxybenzene;4-bromo-2,6-difluorophenyl methyl ether;4-Bromo-2,6-difluorophenyl methyl ether, 5-Bromo-1,3-difluoro-2-methoxybenzene;104197-14-0
• CAS NO: 104197-14-0
• Molecular Formula: C₇H₅BrF₂O
• Molecular Weight: 223.0148064
• Mol File: 104197-14-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 80-100°C 15mm
• Flash Point: 80-100°C/15mm
• Appearance: /
• Density: 1.65
• Vapor Pressure: 0.469mmHg at 25°C
• Refractive Index: 1.5100
• Storage Temp.: Store Cold
• Water Solubility: Insoluble in water.
• Sensitive: Light Sensitive
• CAS DataBase Reference: 4-Bromo-2,6-difluoroanisole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-2,6-difluoroanisole(104197-14-0)
• EPA Substance Registry System: 4-Bromo-2,6-difluoroanisole(104197-14-0)

Safety Data

• Hazard Codes: Xi,F
• Statements: 36/37/38
• Safety Statements: 26-36
• HazardClass: IRRITANT
• Hazardous Substances Data: 104197-14-0(Hazardous Substances Data)

Usage

Chemical Properties

light yellow liquid

Uses

t is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.

InChI:InChI=1/C7H5BrF2S/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H3

Upstream product

• 67-56-1 methanol 
• 138526-69-9 3,4,5-trifluoro-1-bromobenzene 
• 28177-48-2 2,6-difluorophenol 
• 104197-13-9 4-bromo-2,6-difluorophenol 
• 74-88-4 methyl iodide 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 363-47-3 3,5-difluoro-4-methoxyaniline 

Relevant articles and documents

Method for preparing alkyloxy aromatic compound from fluoroaromatic compound

The invention discloses a method for preparing an alkyloxy aromatic compound from a fluoroaromatic compound. The alkyloxy aromatic compound is highly-efficiently prepared through a reaction of the fluoroaromatic compound, a strong alkali, dimethyl sulfoxide and alcohol under certain conditions. The method has the advantages of no metal catalyst, mild and controllable reaction, simple process, good universality, and suitableness for large-scale industrial production.

New oxabispidine compounds for the treatment of cardiac arrhythmias

There is provided compounds of formula I, wherein R1, R2, R3, R41 to R46, X, Y and Z have meanings given in the description, which compounds are useful in the prophylaxis and in the treatment of arrhythmias, in particular atrial and ventricular arrhythmias.

Elemental fluorine Part 12. Fluorination of 1,4-disubstituted aromatic compounds

Direct fluorination of a series of 1,4-disubstituted benzene derivatives in acid reaction media at convenient temperature leads, in many cases, to selectively fluorinated aromatic products in preparatively useful conversions and yields.