Basic information Application Safety Supplier Related

5-Fluoro-2-methoxyphenol

Basic information Application Safety Supplier Related

5-Fluoro-2-methoxyphenol Basic information

Product Name:
5-Fluoro-2-methoxyphenol
Synonyms:
  • 4-fluoro-2-hydroxyanisole
  • 5-FLUORO-2-METHOXYPHENOL
  • 5-fluoro-2-metoxyphenol
  • 5-Fluoro-2-methoxyphenol98%
  • 2-Hydroxy-4-fluoroanisole
  • 2-Hydroxy-4-fluoroanisole, 4-Fluoro-2-hydroxyphenyl methyl ether, 5-Fluoroquaiacol
  • 2-Hydroxy-4-fluoroanisole, 4-Fluoro-2-hydroxyphenyl methyl ether, 5-Fluoroguaiacol
  • 2-Hydroxy-4-fluoroanisole, 5-Fluoroguiacol
CAS:
72955-97-6
MF:
C7H7FO2
MW:
142.13
Product Categories:
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Fluorine Compounds
  • Phenols
  • Aromatic Phenols
  • Phenol&Thiophenol&Mercaptan
Mol File:
72955-97-6.mol
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5-Fluoro-2-methoxyphenol Chemical Properties

Boiling point:
223°C
Density 
1.224
Flash point:
111°C
storage temp. 
2-8°C
form 
liquid
pka
8.97±0.10(Predicted)
color 
Clear
InChI
InChI=1S/C7H7FO2/c1-10-7-3-2-5(8)4-6(7)9/h2-4,9H,1H3
InChIKey
PPJKLEQAFZWIQY-UHFFFAOYSA-N
SMILES
C1(O)=CC(F)=CC=C1OC
CAS DataBase Reference
72955-97-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39
WGK Germany 
WGK 3
Hazard Note 
Irritant
HS Code 
2909500090
Storage Class
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Oral
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5-Fluoro-2-methoxyphenol Usage And Synthesis

Application

5-Fluoro-2-methoxyphenol is an important pesticide and pharmaceutical intermediate. It can be synthesized from methyl ether using butyllithium and trimethoxyboron in the presence of butyllithium and trimethoxyboron. It is used to synthesize alicylates, a drug for treating hypertension.

Synthesis

In a 500 mL four-necked flask add 150 g (0.9 mol) acetyl guaiacol, glacial acetic acid 240 mL, iodine 2.5 g (0.01 mol) at 25 ?? C, stirring dropwise addition of liquid bromine 160 g (2 mol), dropwise addition is complete, heated to 100 ?? C reaction for 10 h, the reaction mixture was cooled to room temperature, with 3000 mL of ethyl acetate was extracted twice, combined with ethyl acetate layer; washed with 500 mL saturated sodium sulfite, then washed with 500 mL saturated saline, recovery of ethyl acetate to obtain the crude product, light yellow colloidal 180.0 g, light yellow colloidal material. The reaction mixture was cooled to room temperature, extracted with 3000 mL of ethyl acetate twice, combined with the ethyl acetate layer, washed with 500 mL of saturated sodium sulfite, then washed with 500 mL of saturated saline, recovered ethyl acetate to obtain the crude product, light yellow colloidal 180.0 g, purity 98.3%, yield 80.2%.

5-Fluoro-2-methoxyphenolSupplier

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