Skip to Content
MilliporeSigma
All Photos(1)

Documents

518786

Sigma-Aldrich

4-Hydroxy-3-methoxyphenylboronic acid pinacol ester

98%

Synonym(s):

2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, 4-Hydroxy-3-methoxyphenylboronic acid, pinacol cyclic ester

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C13H19BO4
CAS Number:
Molecular Weight:
250.10
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

105-109 °C (lit.)

SMILES string

COc1cc(ccc1O)B2OC(C)(C)C(C)(C)O2

InChI

1S/C13H19BO4/c1-12(2)13(3,4)18-14(17-12)9-6-7-10(15)11(8-9)16-5/h6-8,15H,1-5H3

InChI key

WFSJROCEOJANPD-UHFFFAOYSA-N

Application

4-Hydroxy-3-methoxyphenylboronic acid pinacol ester can be used as a reactant:
  • In the Suzuki-Miyaura cross-coupling reaction.
  • To prepare ethylidenedihydroindolones as potential neoplastic agents.
  • To synthesize 5,6-dihydropyrrolo[2,1-b]isoquinoline derivatives, which can be utilized as scaffolds to prepare lamellarin analogs via regioselective bromination and Suzuki cross-coupling reactions.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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

5, 6-Dihydropyrrolo [2, 1-b] isoquinolines as scaffolds for synthesis of lamellarin analogues
Olsen CA, et al.
Tetrahedron Letters, 46(12), 2041-2044 (2005)
New oxidative labels for electrochemical detection of DNA
Simonova A, et al.
Collection of Czechoslovak Chemical Communications, 14, 365-366 (2015)
Synthesis and biological evaluation of 3-ethylidene-1, 3-dihydro-indol-2-ones as novel checkpoint 1 inhibitors
L Nan-Horng, et al.
Bioorganic & Medicinal Chemistry Letters, 16(2), 421-426 (2006)

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