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676624

5-Methoxy-3-pyridineboronic acid pinacol ester

Name: 5-Methoxy-3-pyridineboronic acid pinacol ester
Brand: ALDRICH

97%

Synonym(s):

(3-Methoxypyridin-5-yl)boronic acid pinacol ester, (5-Methoxypyridin-3-yl)boronic acid pinacol ester, 2-(5-Methoxypyridin-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyridine, 3-Methoxy-5-(pinacolboranato)pyridine, 5-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) pyridine

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About This Item

Empirical Formula (Hill Notation):

C₁₂H₁₈BNO₃

CAS Number:

445264-60-8

Molecular Weight:

235.09

NACRES:

NA.22

PubChem Substance ID:

24884859

UNSPSC Code:

12352103

MDL number:

MFCD03412068

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Properties

assay

97%

form

solid

mp

100-108 °C

SMILES string

COc1cncc(c1)B2OC(C)(C)C(C)(C)O2

InChI

1S/C12H18BNO3/c1-11(2)12(3,4)17-13(16-11)9-6-10(15-5)8-14-7-9/h6-8H,1-5H3

InChI key

HENXUFOAGXNWKH-UHFFFAOYSA-N

Description

Application

5-Methoxy-3-pyridineboronic acid pinacol ester can be used:

To synthesize anthracene based bis-pyridine ligand (L), which is employed in the preparation of fluorescent M₂L₄ type capsules (M= Pt, Zn, Pd, Cu, Ni, Co, and Mn).
As a starting material in the synthesis of pyridylmethyl pyridine derivatives as potent 11β-hydroxylase (CPY11B1) inhibitors.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Isostructural M2L4 molecular capsules with anthracene shells: synthesis, crystal structures, and fluorescent properties

Li Z, et al.

Chemistry?A European Journal , 18(27), 8358-8365 (2012)

Accelerated skin wound healing by selective 11β-hydroxylase (CYP11B1) inhibitors

Emmerich J, et al.

European Journal of Medicinal Chemistry, 143(27), 591-597 (2018)

Cushing?s syndrome: Development of highly potent and selective CYP11B1 inhibitors of the (pyridylmethyl) pyridine type