Skip to Content
Merck
All Photos(1)

Key Documents

720828

Sigma-Aldrich

Indazole-6-boronic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C7H7BN2O2
CAS Number:
Molecular Weight:
161.95
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

form

solid

mp

112-117 °C

storage temp.

2-8°C

SMILES string

OB(O)c1ccc2cn[nH]c2c1

InChI

1S/C7H7BN2O2/c11-8(12)6-2-1-5-4-9-10-7(5)3-6/h1-4,11-12H,(H,9,10)

InChI key

ZKNLCHWRWRYPGG-UHFFFAOYSA-N

Application

Indazole-6-boronic acid can be used as a reactant:
  • In Suzuki-Miyaura coupling reaction to synthesize indazole derivatives via C-C bond formation by reacting with different aryl halides.
  • To synthesize indazole substituted purines and pyrrolo[2,3-d]pyrimidines as potential kinase inhibitors.

Reactant for preparation of:
  • Bicyclic hydroxyphenylmethanone derivatives as hydroxysteroid dehydrogenase inhibitors
  • Bisphosphonate inhibitors of human farnesyl pyrophosphate synthase
  • Indazolyl benzoimidazoles as PKC-ζ inhibitors
  • Pyrazolopyrimidinamine derivatives and their tyrosine and phosphinositide kinase inhibitory activity

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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