Skip to Content
Merck
CN

518808

Bis(neopentyl glycolato)diboron

96%

Synonym(s):

5,5,5′,5′-Tetramethyl-2,2′-bi-1,3,2-dioxaborinane

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C10H20B2O4
CAS Number:
201733-56-4
Molecular Weight:
225.89
NACRES:
NA.22
PubChem Substance ID:
24874048
UNSPSC Code:
12352103
MDL number:
MFCD02093062

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Bis(neopentyl glycolato)diboron, 96%

InChI

1S/C10H20B2O4/c1-9(2)5-13-11(14-6-9)12-15-7-10(3,4)8-16-12/h5-8H2,1-4H3

SMILES string

CC1(C)COB(OC1)B2OCC(C)(C)CO2

InChI key

MDNDJMCSXOXBFZ-UHFFFAOYSA-N

assay

96%

mp

180.5-184.5 °C (lit.)

Quality Level

100

Related Categories

Application

Reagent to prepare boronic acid esters.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCN8513
MKCL9190
MKCK7882
MKCC1139
MKBT8538V

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

George W Kabalka et al.
Nuclear medicine and biology, 30(4), 369-372 (2003-05-28)
A direct radioiodination of (Z)-vinylboronic acid esters to the corresponding vinyl iodides using Na(123)I and chloramine-T is described. The boronates were prepared from vinyl iodides via palladium coupling reactions.

Articles

Rapid Arylboronic Esters Synthesis by Ir(I)-Catalysis

Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.

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