CAS 230299-21-5 Bis(hexylene glycolato)diboron

NAVIGATION

Bis(hexylene glycolato)diboron

PRICE INQUIRY

Catalog Number

ACM230299215-2

CAS Number

230299-21-5

Product Name

Bis(hexylene glycolato)diboron

Category

Salt

Synonyms

4,4,6-TRIMETHYL-2-(4,4,6-TRIMETHYL-1,3,2-DIOXABORINAN-2-YL)-1,3,2-DIOXABORINANE;4,4,4,4,6,6-HEXAMETHYL-2,2-BI-1,3,2-DIOXABORINANE;BIS(2-METHYL-2,4-PENTANEDIOLATO)DIBORON;BIS(1,3,3-TRIMETHYL-1,3-PROPANEDIOLATO)DIBORON;BIS(HEXYLENE GLYCOLATO)DIBORON;Bis(hex

IUPAC Name

4,4,6-trimethyl-2-(4,4,6-trimethyl-1,3,2-dioxaborinan-2-yl)-1,3,2-dioxaborinane

Molecular Weight

253.9g/mol

Molecular Formula

C12H24B2O4

Canonical SMILES

B1(OC(CC(O1)(C)C)C)B2OC(CC(O2)(C)C)C

InChI

InChI=1S/C12H24B2O4/c1-9-7-11(3,4)17-13(15-9)14-16-10(2)8-12(5,6)18-14/h9-10H,7-8H2,1-6H3

InChI Key

UEBSWKNVDRJVHN-UHFFFAOYSA-N

Purity

98%

Application

Bis(hexylene glycolato)diboron serves as a versatile reagent in several organic synthesis processes. It is employed in the preparation of aryl boronate esters through metal-catalyzed direct C-H borylation of aryl compounds. Additionally, it is instrumental in the chemoselective synthesis of C-C coupling products, facilitated by nickel-catalyzed coupling of primary and secondary alkyl halides. Furthermore, this compound is utilized in the nickel-catalyzed regioselective arylboration of terminal nonactivated alkenes, resulting in the formation of alkyl boranes.

Complexity

279

Covalently-Bonded Unit Count

Exact Mass

254.18607g/mol

Formal Charge

Heavy Atom Count

Monoisotopic Mass

254.18607g/mol

Rotatable Bond Count

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