Basic information Safety Supplier Related

2-Fluoro-6-methoxyphenylboronic acid

Basic information Safety Supplier Related

2-Fluoro-6-methoxyphenylboronic acid Basic information

Product Name:
2-Fluoro-6-methoxyphenylboronic acid
Synonyms:
  • 2-FLUORO-6-METHOXYPHENYLBORONIC ACID
  • 2-FLUORO-6-METHOXYLPHENYLBORONIC ACID
  • 2-Fluoro-6-Methoxyphenylboroni
  • 2-Fluoro-6-methoxybenzeneboronic acid 96%
  • 2-Fluoro-6-methoxybenzeneboronicacid96%
  • 3-Fluoroanisole-2-boronic acid
  • 2-Fluoro-6-methoxyph
  • 2-Borono-3-fluoroanisole
CAS:
78495-63-3
MF:
C7H8BFO3
MW:
169.95
Product Categories:
  • Aryl Boronic Acids
  • Boronic Acids and Derivatives
  • Alkoxy
  • Chemical Synthesis
  • Disubstituted Aryl Boronic Acids
  • Organometallic Reagents
  • blocks
  • BoronicAcids
  • Aryl
  • Organoborons
  • Boronic acid
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Boronic Acids
  • FluoroCompounds
Mol File:
78495-63-3.mol
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2-Fluoro-6-methoxyphenylboronic acid Chemical Properties

Melting point:
120-125 °C (lit.)
Boiling point:
303.1±52.0 °C(Predicted)
Density 
1.26±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
8.35±0.58(Predicted)
color 
White to Off-White
InChI
InChI=1S/C7H8BFO3/c1-12-6-4-2-3-5(9)7(6)8(10)11/h2-4,10-11H,1H3
InChIKey
XOVMDVZAWWQSDC-UHFFFAOYSA-N
SMILES
B(C1=C(OC)C=CC=C1F)(O)O
CAS DataBase Reference
78495-63-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36/37/39-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2931900090

MSDS

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2-Fluoro-6-methoxyphenylboronic acid Usage And Synthesis

Uses

Reactant for:• ;Preparation of functionally selective allosteric modulators of GABAA receptors1• ;Suzuki cross-coupling reaction2,3• ;Preparation of inhibitors of the checkpoint kinase Wee14

Uses

suzuki reaction

Uses

2-Fluoro-6-methoxyphenylboronic Acid is a boronic acid derivative known for its pharmacological activity and utility as intermediates in the synthesis of novel non-boron containing compounds, and potential bacterial mutagens.

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