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Merck
CN

720828

Sigma-Aldrich

吲唑-6-硼酸

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About This Item

经验公式(希尔记法):
C7H7BN2O2
分子量:
161.95
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

表单

solid

质量水平

mp

112-117 °C

储存温度

2-8°C

SMILES字符串

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

应用

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Design and synthesis of active site inhibitors of the human farnesyl pyrophosphate synthase: apoptosis and inhibition of ERK phosphorylation in multiple myeloma cells
Lin Y-S, et al.
Journal of medicinal chemistry, 55(7), 3201-3215 (2012)
Design, synthesis, and preclinical evaluation of fused pyrimidine-based hydroxamates for the treatment of hepatocellular carcinoma
Chen D, et al.
Journal of Medicinal Chemistry, 61(4), 1552-1575 (2018)

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