CAS 13826-27-2: bis(catecholato)diboron
Formula:C12H8B2O4
InChI:InChI=1/C12H8B2O4/c1-2-6-10-9(5-1)15-13(16-10)14-17-11-7-3-4-8-12(11)18-14/h1-8H
SMILES:c1ccc2c(c1)OB(B1Oc3ccccc3O1)O2
Synonyms:- 2,2'-Bi-1,3,2-benzodioxaborole
- 2-(1,3,2-Benzodioxaborol-2-Yl)-1,3,2-Benzodioxaborole
- 2,2'-Bis-1,3,2-Benzodioxaborole
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Found 5 products.
2,2'-Bibenzo[d][1,3,2]dioxaborole
CAS:Purity:95.0%Color and Shape:Solid, Crystalline or PowderMolecular weight:237.80999755859375Bis(catecholato)diborane
CAS:Bis(catecholato)diboraneFormula:C12H8B2O4Purity:By gc: 98.7% by area (Typical Value in Batch COA)Color and Shape: white solidMolecular weight:237.81g/molBis(catecholato)diboron
CAS:Formula:C12H8B2O4Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:237.812,2'-Bi-1,3,2-benzodioxaborole
CAS:Formula:C12H8B2O4Purity:98%Color and Shape:SolidMolecular weight:237.8115Bis(catecholato)diboron
CAS:Bis(catecholato)diboron is a boron compound with the formula B(OCHCOOH). It is a colorless solid that reacts with acids to form the corresponding esters. The trifluoroacetate anion, BFOCO- can be used as a nucleophile in organic synthesis reactions. This reaction mechanism is catalyzed by acid or base. Bis(catecholato)diboron has been shown to be a good catalyst for coupling reactions of hydroxy group radicals with alkoxy radicals, which are synthesized from fatty acids and alcohols. The yield of this reaction is high, typically greater than 90%.Formula:C12H8B2O4Purity:Min. 95%Molecular weight:237.81 g/mol
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