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721352

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

Name: 3,6-Dihydro-2<I>H</I>-pyran-4-boronic acid pinacol ester
Brand: ALDRICH

97%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):

C₁₁H₁₉BO₃

CAS Number:

287944-16-5

Molecular Weight:

210.08

NACRES:

NA.22

PubChem Substance ID:

329763842

UNSPSC Code:

12352103

MDL number:

MFCD11052631

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Properties

Quality Level

100

assay

97%

form

solid

mp

63-67 °C

functional group

ether

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

Description

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

GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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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)

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)

Optimization of permeability in a series of pyrrolotriazine inhibitors of IRAK4

Degorce SL, et al.

Bioorganic & Medicinal Chemistry, 26(4), 913-924 (2018)

Global Trade Item Number

SKU	GTIN
721352-1G	04061826263891