1-Bromo-3,5-difluorobenzene
1-Bromo-3,5-difluorobenzene Basic information
- Product Name:
- 1-Bromo-3,5-difluorobenzene
- Synonyms:
-
- 1-Bromo-3,5-difluorobenzene,99%
- 1-BROMO-3,5-DIFLUOROBENZENE
- 3,5-DIFLUOROBROMOBENZENE
- 1-Bromo-3,5-difluorobenzene,98% [3,5-Difluorobromobenzene]
- 3,5-difluoro-1-bromobenzene
- 1-Bromo-3,5-difluorobenzene 98%
- 1-Bromo-3,5-difluorobenzene98%
- 1-Brom-3,5-difluorbenzol
- CAS:
- 461-96-1
- MF:
- C6H3BrF2
- MW:
- 192.99
- EINECS:
- 416-710-2
- Product Categories:
-
- Fluorine series
- Fluorobenzene
- Miscellaneous
- Aryl
- Halogenated Hydrocarbons
- Aromatic Hydrocarbons (substituted) & Derivatives
- bc0001
- C6
- Mol File:
- 461-96-1.mol
1-Bromo-3,5-difluorobenzene Chemical Properties
- Melting point:
- -27 °C
- Boiling point:
- 140 °C (lit.)
- Density
- 1.676 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.499(lit.)
- Flash point:
- 112 °F
- storage temp.
- Sealed in dry,2-8°C
- solubility
- 0.238g/l
- form
- Liquid
- color
- Clear colorless to light yellow
- Specific Gravity
- 1.686
- PH
- 6.6 (0.238g/l, H2O, 20℃)
- Water Solubility
- 0.238 g/L (20 ºC)
- BRN
- 1931520
- InChIKey
- JHLKSIOJYMGSMB-UHFFFAOYSA-N
- CAS DataBase Reference
- 461-96-1(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xn,N,F,Xi
- Risk Statements
- 10-22-38-43-48/22-50/53-36/37/38
- Safety Statements
- 24-36/37-60-61-36-26-16
- RIDADR
- UN 1993 3/PG 3
- WGK Germany
- 2
- Hazard Note
- Flammable
- HazardClass
- 3
- PackingGroup
- III
- HS Code
- 29039990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
1-Bromo-3,5-difluorobenzene Usage And Synthesis
Chemical Properties
CLEAR COLOURLESS TO LIGHT YELLOW LIQUID
Uses
1-Bromo-3,5-difluorobenzene was used in the synthesis of 4-bromo-2,6-difluorobenzoic acid.
Uses
Intermediates of Liquid Crystals
Synthesis Reference(s)
Journal of Medicinal Chemistry, 30, p. 486, 1987 DOI: 10.1021/jm00386a008
Synthesis
6303-21-5
101471-20-9
461-96-1
General procedure: A diazonium salt solution was prepared by dissolving 1 mole of 2-bromo-4,6-difluoroaniline hydrobromide in aqueous HCl with 1.1-1.10 moles of NaNO2 at 0°C to 5°C. The solution was then slowly warmed to 15°C, during which time the release of nitrogen was observed. To this solution, 1.5 moles of hypophosphorous acid was added at a temperature below 5°C, followed by a slow warming to 15°C, during which the release of nitrogen was observed. The reaction mixture is stirred for 1 hour, decanted and extracted with a suitable organic solvent to give 1-bromo-3,5-difluorobenzene in 75% molar yield. The target product with purity higher than 99% was obtained by distillation. This method is also applicable to the synthesis of other 1-bromo-3,5-dihalobenzenes.
References
[1] Patent: US5157169, 1992, A
1-Bromo-3,5-difluorobenzene Preparation Products And Raw materials
Raw materials
Preparation Products
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1-Bromo-3,5-difluorobenzene(461-96-1)Related Product Information
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- 1,2-DIBROMO-3,5-DIFLUOROBENZENE
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