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2,3-Difluorophenol

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2,3-Difluorophenol Basic information

Product Name:
2,3-Difluorophenol
Synonyms:
  • 2,3-DIFLUOROPHENOL
  • PHENOL, 2,3-DIFLUORO-
  • 2,3-Difluorophenol,98+%
  • 2,3-Difluorophenole
  • 2,3-Difluorophenol 98%
  • Difluorophenol
  • 2,3-Difluorophenol 6418-38-8 fiona
  • 2,3-Difluorophenol ,99%
CAS:
6418-38-8
MF:
C6H4F2O
MW:
130.09
EINECS:
264-750-2
Product Categories:
  • Phenyls & Phenyl-Het
  • Indolines ,Indoles ,Indazoles
  • Organic Building Blocks
  • Oxygen Compounds
  • Phenols
  • Fluorine series
  • Phenyls & Phenyl-Het
  • Phenol&Thiophenol&Mercaptan
  • Miscellaneous
  • Fluorophenols
  • Aromatic Halides (substituted)
  • Fluorobenzene
  • Alcohols and Derivatives
  • Trifluoromethoxybenzene Series
  • Other fluorin-contained compounds
  • bc0001
Mol File:
6418-38-8.mol
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2,3-Difluorophenol Chemical Properties

Melting point:
39-42 °C (lit.)
Boiling point:
54 °C/25 mmHg (lit.)
Density 
1.2483 (estimate)
Flash point:
134 °F
storage temp. 
Inert atmosphere,2-8°C
pka
7.71±0.10(Predicted)
form 
powder to lump to clear liquid
color 
White or Colorless to Almost white or Almost colorless
BRN 
2082265
InChI
InChI=1S/C6H4F2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H
InChIKey
RPEPGIOVXBBUMJ-UHFFFAOYSA-N
SMILES
C1(O)=CC=CC(F)=C1F
CAS DataBase Reference
6418-38-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
F,Xn,Xi,C
Risk Statements 
11-22-36/37/38-34-20/21/22
Safety Statements 
26-45-36/37/39-16
RIDADR 
UN 1325 4.1/PG 2
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
4.1
PackingGroup 
III
HS Code 
29081000

MSDS

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2,3-Difluorophenol Usage And Synthesis

Chemical Properties

white crystalline low melting mass

Uses

Intermediates of Liquid Crystals

Application

2,3-Difluorophenol was used in the synthesis of material-poly{methyl[3-(2-hydroxy-3,4-difluoro)phenyl]propyl siloxane} (PMDFPS) sensitive to toxic organophosphate.

Synthesis

121219-16-7

6418-38-8

Step 1: In a 500 mL round-bottomed flask, dissolve 2,3-difluorophenylboronic acid (30 g, 189.98 mmol, 1.00 eq.) in dichloromethane (250 mL). Hydrogen peroxide (30 mL) was added slowly and dropwise under stirring conditions. The reaction mixture was stirred continuously at 25°C for 2 hours. Upon completion of the reaction, the reaction mixture was washed sequentially with water and saturated saline, the organic phase was dried over anhydrous magnesium sulfate, and subsequently concentrated under reduced pressure to afford 2,3-difluorophenol 23 g (93% yield) as a brown oil.

References

[1] K.P. RAJAPPAN NAIR . Supersonic jet microwave rotational spectrum of 2,3-difluorophenol[J]. Journal of Molecular Structure, 2019, 1195: Pages 479-484. DOI:10.1016/j.molstruc.2019.06.004.
[2] WEI HE . Analytical application of poly{methyl[3-(2-hydroxy-3,4-difluoro)phenyl]propyl siloxane} as a QCM coating for DMMP detection[J]. Talanta, 2008, 76 3: Pages 698-702. DOI:10.1016/j.talanta.2008.04.022.
[3] E. MARZI M. S J Gorecka. The regioexhaustive functionalization of difluorophenols and trifluorophenols through organometallic intermediates[J]. Synthesis-Stuttgart, 2004, 441 1: 1609-1618. DOI:10.1055/S-2004-829110.

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