188913
Catecholborane
98%
Synonym(s):
Catecholatoborane, Catecholborane (CB), Pyrocatecholborane
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About This Item
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Quality Level
Assay
98%
form
liquid
reaction suitability
reagent type: reductant
refractive index
n20/D 1.507 (lit.)
bp
50 °C/50 mmHg (lit.)
mp
12 °C (lit.)
density
1.125 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
[bH]1oc2ccccc2o1
InChI
1S/C6H5BO2/c1-2-4-6-5(3-1)8-7-9-6/h1-4,7H
InChI key
CENMEJUYOOMFFZ-UHFFFAOYSA-N
Application
A monofunctional hydroborating agent which reduces β-hydroxyketones to 1,3-diols. Effects conjugate reduction of α,β-enones.
Used to prepare B-alkylcatecholboranes which were used, in turn, to generate alkyl radicals forming aryl ethers from quinones. Employed in a preparation of C2-symmetric boron complexes from methylenebis(oxazolines) used for enantioselective reduction of ketones.
Legal Information
Made under U.S. Pat. No. 6,204,405.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
35.6 °F - closed cup
Flash Point(C)
2 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The Journal of Organic Chemistry, 55, 5678-5678 (1990)
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Organic letters, 8(25), 5861-5864 (2006-12-01)
Addition of alkyl radicals generated from B-alkylcatecholboranes onto 1,4-benzoquinones leads to substituted hydroquinones in good overall yields. Formation of aryl ethers via a unique radical addition to the oxygen atom of the enone system is the main reaction when bulky
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