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3-FLUORO-O-XYLENE

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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
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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)
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Safety Information

Hazard Codes 
F,Xi
Risk Statements 
10-37
Safety Statements 
16-24/25
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
RTECS 
ZE4560000
Hazard Note 
Flammable
HazardClass 
3
PackingGroup 
III
HS Code 
29039990

MSDS

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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

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