2,6-Difluorophenylboronic acid
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2,6-Difluorophenylboronic acid is an ortho-substituted phenylboronic acid bearing two fluorine substituents at the 2- and 6-positions, and it serves as an arylboron substrate in Suzuki-Miyaura coupling reactions. 2,6-Difluorophenylboronic acid is used in organic synthesis-related research.
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- Pureté : 99.74%
- CAS No.: 162101-25-9
- Formule: C6H5BF2O2
- Masse moléculaire:157.91
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Stockage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
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Activité biologique
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Chemical Information
- Pureté et documentation
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Help & FAQs
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Activité biologique
Description
In Vitro
2,6-Difluorophenylboronic acid is prone to protodeboronation; ortho-fluoro substituents accelerate the protodeboronation of arylboronic acids[1].
2,6-Difluorophenylboronic acid serves as an arylboronic acid substrate in the copper-mediated arylation of selenocysteine, yielding the corresponding arylated selenocysteine polypeptide product[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
Chemical Information
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CAS No. 162101-25-9
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Appearance Solid
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Masse moléculaire 157.91
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Formule C6H5BF2O2
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Color White to off-white
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SMILES
FC1=C(B(O)O)C(F)=CC=C1
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Pureté et documentation
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Fiche technique (269 KB)
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SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
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Instruction de manipulation (2659 KB)
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
2,6-Difluorophenylboronic acid Related Classifications
HY-32885 Related Classifications
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