3-FLUORO-O-XYLENE
3-FLUORO-O-XYLENE Basic information
- Product Name:
- 3-FLUORO-O-XYLENE
- Synonyms:
-
- 3-fluoro-o-xylen
- Benzene, 1-fluoro-2,3-dimethyl-
- o-Xylene, 3-fluoro-
- 3-FLUORO-1,2-XYLENE
- 3-FLUORO-1,2-DIMETHYL BENZENE
- 3-FLUORO-O-XYLENE
- 1,2-DIMETHYL-3-FLUOROBENZENE
- 1-FLUORO-2,3-DIMETHYLBENZENE
- CAS:
- 443-82-3
- MF:
- C8H9F
- MW:
- 124.16
- EINECS:
- 207-140-3
- Product Categories:
-
- Halogen toluene
- Mol File:
- 443-82-3.mol
3-FLUORO-O-XYLENE Chemical Properties
- Boiling point:
- 148-152 °C(lit.)
- Density
- 0.99 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.486(lit.)
- Flash point:
- 97 °F
- storage temp.
- Sealed in dry,2-8°C
- form
- clear liquid
- color
- Colorless to Almost colorless
- Specific Gravity
- 0.992
- Water Solubility
- Insoluble in water.
- BRN
- 2040955
- CAS DataBase Reference
- 443-82-3(CAS DataBase Reference)
- NIST Chemistry Reference
- 3-Fluoro-o-xylene(443-82-3)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
3-FLUORO-O-XYLENE Usage And Synthesis
Chemical Properties
clear colorless liquid
Uses
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.
Synthesis
87-59-2
443-82-3
Example 5: Synthesis of 2,3-dimethylfluorobenzene 1. Diazotization reaction: 2,3-dimethylaniline (2.3 g, 0.02 mol) was slowly added to Et3N-3HF (30 cm3) at 0 °C. Subsequently, sodium nitrite (2.0 g, 0.03 mol) was added in batches with the aid of ultrasound and significant gas release was observed for about 25 min. The reaction mixture gradually changed from clear to yellow and finally to dark color due to tar generation. 2. Post-treatment: the brown reaction mixture was poured into water (150 cm3) and extracted with ether (180 cm3 x 2). The remaining tar-like substance was transferred to Soxhlet extractor and extracted continuously with ether (30cm3) for 24 hours. All the ether extracts were combined and dried with magnesium sulphate and subsequently the ether was removed by fractional distillation to give a brown oily substance. 3. purification: the above oily substance was distilled at 142-143°C (atmospheric pressure) to give 1-fluoro-2,3-dimethylbenzene (1.47 g, 63.4% yield) as a clear liquid. 4. Characterization: - 1H NMR (CDCl3) δ: 2.18 (d, J = 2.0 Hz, 3H, 2-CH3), 2.28 (s, 3H, 3-CH3), 6.88 (t, J = 7.6 Hz, 1H, 6-H), 6.91 (d, J = 7.6 Hz, 1H, 4-H), 7.03 (q, J = 8.0 Hz and J = 6.0 Hz, 1H, 5 -H). - 19F NMR (CDCl3) δ: 118.3 (tq, J = 7.6Hz and J = 2.0Hz, 1-F). - Mass spectrum: molecular ion peak at m/z 124, and fragmentation peaks at m/z 109, 101, 96, 86, 83 and 77, consistent with the expected fragmentation pattern of 1-fluoro-2,3-dimethylbenzene.
References
[1] Patent: US6179970, 2001, B2
[2] Journal of the Chemical Society. Perkin Transactions 1, 2002, # 3, p. 402 - 415
[3] Proceedings - Indian Academy of Sciences, Section A, 1959, vol. 50, p. 51,56, 58, 59
[4] Journal of Organic Chemistry, 1961, vol. 26, p. 3208 - 3211
3-FLUORO-O-XYLENESupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
- Tel
- 0311-89250318 031166536426
- master@sjzsdyn.com
3-FLUORO-O-XYLENE(443-82-3)Related Product Information
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZYLAMINE
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZONITRILE
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZOPHENONE
- 3-Fluorophthalic anhydride
- 3-Fluoro-2-methylbenzaldehyde
- Tetrafluorophthalic anhydride
- 3-FLUORO-O-XYLENE
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZYL BROMIDE
- 3-Fluorophthalic acid
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZYL ALCOHOL
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZOYL CHLORIDE
- 3-FLUORO-2-METHYLBENZOIC ACID
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZALDEHYDE
- 3,4,5,6-Tetrafluorophthalonitrile
- Tetrafluorophthalic acid
- 2-FLUORO-6-(TRIFLUOROMETHYL)BENZOIC ACID
- 3-Bromo-4-chloropyridine
- 3,6-DIFLUOROPHTHALIC ANHYDRIDE