2-BROMO-1,3,2-BENZODIOXABOROLE
2-BROMO-1,3,2-BENZODIOXABOROLE Basic information
- Product Name:
- 2-BROMO-1,3,2-BENZODIOXABOROLE
- Synonyms:
-
- B-BROMOCATECHOLBORANE
- 2-BROMO-1,3,2-BENZODIOXABOROLE
- beta-Bromocatecholborane
- 2-bromo-1,3,2-benzodioxaborale
- Catechol boron bromide
- o-Phenylene bromoboronate
- B-Bromocatecholborane
- 1,3,2-Benzodioxaborole, 2-bromo-
- CAS:
- 51901-85-0
- MF:
- C6H4BBrO2
- MW:
- 198.81
- Product Categories:
-
- B (Classes of Boron Compounds)
- B-Bromocatecholborane, etc.
- Mol File:
- 51901-85-0.mol
2-BROMO-1,3,2-BENZODIOXABOROLE Chemical Properties
- Melting point:
- 51-53 °C(lit.)
- Boiling point:
- 76 °C9 mm Hg(lit.)
- Density
- 1.67±0.1 g/cm3(Predicted)
- Flash point:
- 107 °F
- storage temp.
- 2-8°C
- solubility
- sol dichloromethane
- form
- powder to lump
- color
- White to Amber to Dark purple
- BRN
- 2445073
- CAS DataBase Reference
- 51901-85-0
Safety Information
- Hazard Codes
- C
- Risk Statements
- 14-34-37
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 2925 4.1/PG 2
- WGK Germany
- 3
- F
- 8-10-21
- HS Code
- 2931.90.6000
- HazardClass
- 4.1
- PackingGroup
- III
MSDS
- Language:English Provider:SigmaAldrich
2-BROMO-1,3,2-BENZODIOXABOROLE Usage And Synthesis
Uses
B-Bromocatecholborane is a mild Lewis acid capable of selective cleavage of ether, ester and carbamate protecting groups; catalyst for Diels-Alder reactions.
Preparation
B-Bromocatecholborane can be conveniently prepared by treating Catechol with Boron Tribromide. The reagent is isolated by distillation as a moisture-sensitive, low-melting solid.
storage
B-Bromocatecholborane is a flammable solid, moisture sensitive; may be conveniently stored and dispensed as a 0.2 M solution in dichloromethane. If properly protected from moisture, these solutions are stable for a period of months[1]. Use in a fume hood.
Purification Methods
Keep at 20o/15mm for some time and then fractionally distil. [Gerrard J Chem Soc 1529 1959, Beilstein 6 IV 5612.]
References
1. Boeckman Jr., R. K.; Potenza, J. C. TL 1985, 26, 1411.
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