Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

525685

Sigma-Aldrich

Bis(hexylene glycolato)diboron

96%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12H24B2O4
CAS Number:
230299-21-5
Molecular Weight:
253.94
MDL number:
MFCD06246008
UNSPSC Code:
12352103
PubChem Substance ID:
24874501
NACRES:
NA.22

Quality Level

100

Assay

96%

mp

98-102 °C (lit.)

SMILES string

CC1CC(C)(C)OB(O1)B2OC(C)CC(C)(C)O2

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

Related Categories

Application

Bis(hexylene glycolato)diboron can be used as a reagent:
  • To prepare aryl boronate esters via metal-catalyzed direct C-H borylation of aryl compounds.
  • In the chemoselective synthesis of C−C coupling products via nickel catalyzed coupling of primary and secondary alkyl halides.
  • In the nickel-catalyzed regioselective arylboration of terminal nonactivated alkenes to yield alkyl boranes.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

525685-BULK:
525685-1G:
525685-VAR:
525685-5G:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
04124AI
07209TU

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Benzene-1,4-diboronic acid ≥95.0%

Sigma-Aldrich

417130

Benzene-1,4-diboronic acid

Nickel-catalyzed cross-coupling of unactivated alkyl halides using bis (pinacolato) diboron as reductant
X Hailiang, et al.
Chemical Science, 4(10), 4022-4029 (2013)
Borylation of Arenes with Bis (hexylene glycolato) diboron
Liskey CW and Hartwig JF
Synthesis, 45(13), 1837-1842 (2013)
Nickel-Catalyzed Migratory Arylboration of Nonactivated Alkenes
Wang W, et al.
Synlett, 30(16), 1850-1854 (2019)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service