Skip to Content
Merck
All Photos(2)

Documents

721352

Sigma-Aldrich

3,6-Dihydro-2H-pyran-4-boronic acid pinacol ester

97%

Synonym(s):

2-(3,6-Dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H19BO3
CAS Number:
Molecular Weight:
210.08
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

63-67 °C

storage temp.

2-8°C

SMILES string

CC1(C)OB(OC1(C)C)C2=CCOCC2

InChI

1S/C11H19BO3/c1-10(2)11(3,4)15-12(14-10)9-5-7-13-8-6-9/h5H,6-8H2,1-4H3

InChI key

DOSGEBYQRMBTGS-UHFFFAOYSA-N

Application

3,6-Dihydro-2H-pyran-4-boronic acid pinacol ester can be used:
  • To prepare 1,2-dihydro-2-oxopyridine based endocannabinoid system (ECS) modulators.
  • As an intermediate in the synthesis of embryonic ectoderm development (EED) inhibitors.
  • To prepare pyrrolotriazine based IRAK4 inhibitors.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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

EEDi-5285: An Exceptionally Potent, Efficacious, and Orally Active Small-Molecule Inhibitor of Embryonic Ectoderm Development
Rej RK, et al.
Journal of medicinal chemistry, 63(13), 7252-7267 (2020)
Optimization of permeability in a series of pyrrolotriazine inhibitors of IRAK4
Degorce SL, et al.
Bioorganic & Medicinal Chemistry, 26(4), 913-924 (2018)
Modification on the 1, 2-dihydro-2-oxo-pyridine-3-carboxamide core to obtain multi-target modulators of endocannabinoid system
Gado F, et al.
Bioorganic Chemistry, 94, 103353-103353 (2020)

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