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4-Chloro-3-fluorophenol

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4-Chloro-3-fluorophenol Basic information

Product Name:
4-Chloro-3-fluorophenol
Synonyms:
  • 4-Chloro-3-fluorophenol,98%
  • 4-Chloro-3-fluorophenol 98%
  • 3-fluoro-4-chlorophenol
  • 4-CHLORO-3-FLUOROPHENOL
  • 4-Chloro-3-fluorophenol >
  • Phenol, 4-chloro-3-fluoro-
  • 4-Chloro-3-fluorophenol ISO 9001:2015 REACH
CAS:
348-60-7
MF:
C6H4ClFO
MW:
146.55
EINECS:
609-036-7
Product Categories:
  • Fluorine series
  • Phenol&Thiophenol&Mercaptan
  • Chlorine Compounds
  • Fluorine Compounds
  • Phenols
  • Organic Building Blocks
  • Oxygen Compounds
  • Aromatic Phenols
Mol File:
348-60-7.mol
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4-Chloro-3-fluorophenol Chemical Properties

Melting point:
54-56 °C (lit.)
Boiling point:
84 °C/44 mmHg (lit.)
Density 
1.3675 (estimate)
Flash point:
>230 °F
storage temp. 
Inert atmosphere,Room Temperature
solubility 
chloroform: soluble50mg/mL, clear, colorless
pka
8.52±0.18(Predicted)
form 
Liquid
color 
Colorless to pale yellow, may discolor to orange during storage
BRN 
3236440
InChI
InChI=1S/C6H4ClFO/c7-5-2-1-4(9)3-6(5)8/h1-3,9H
InChIKey
XLHYAEBESNFTCA-UHFFFAOYSA-N
SMILES
C1(O)=CC=C(Cl)C(F)=C1
CAS DataBase Reference
348-60-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-37/39-36/37/39-24/25
RIDADR 
2811
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
IRRITANT, IRRITANT-HARMFUL
HazardClass 
8
HS Code 
29081990

MSDS

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4-Chloro-3-fluorophenol Usage And Synthesis

Chemical Properties

White to salmon crystalline solid

Uses

4-Chloro-3-fluorophenol was used in the synthesis of 4-chloro-3-fluoro catechol and 5-Chloro-4-fluoro-2-hydroxyacetophenone.

General Description

4-Chloro-3-fluorophenol is hydroxylated at both ortho positions to yield different products.

Synthesis

1338215-43-2

348-60-7

GENERAL METHOD: [2-(Phenoxy)-ethyl]-trimethyl-silane (195 mg, 1.0 mmol) was dissolved in anhydrous DMF (2 mL), cesium fluoride (576 mg, 3.0 mmol) was added, and the reaction was stirred for 1 hr at 60 °C. After the reaction was completed, the reaction mixture was diluted with water and extracted with ethyl acetate (3 × 20 mL). The organic layers were combined, washed sequentially with water and saturated saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 92 mg of 4-chloro-3-fluorophenol in 93% yield. The 1H NMR data of the compound was consistent with the standard, confirming its structure.

References

[1] ISHIKAWA Y. 6-Chloro-7-fluoro-4-oxo-4H-chromene-3-carbaldehyde.[J]. Acta crystallographica. Section E, Structure reports online, 2014, 70 Pt 7: o825. DOI:10.1107/S1600536814014706.
[2] VIDYA S. SHIVATARE W. T. Vibronic and cation spectroscopy of selected rotamers of 4-chloro-3-fluorophenol[J]. Molecular Physics, 2014, 112 1: 2397-2406. DOI:10.1080/00268976.2014.904050.

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