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766097

Sigma-Aldrich

Isoquinoline-6-boronic acid pinacol ester

95%

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About This Item

Empirical Formula (Hill Notation):
C15H18BNO2
CAS Number:
Molecular Weight:
255.12
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:

Quality Level

assay

95%

form

solid

mp

179-184 °C

storage temp.

2-8°C

SMILES string

CC1(C)OB(OC1(C)C)c2ccc3cnccc3c2

InChI

1S/C15H18BNO2/c1-14(2)15(3,4)19-16(18-14)13-6-5-12-10-17-8-7-11(12)9-13/h5-10H,1-4H3

InChI key

LFALMDZWCMSBFO-UHFFFAOYSA-N

Related Categories

Application

Useful boron compound for Suzuki coupling.

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


Certificates of Analysis (COA)

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Qiuping Wang et al.
Journal of medicinal chemistry, 50(2), 199-210 (2007-01-19)
We describe the biological evaluation of isothiazoloquinolones (ITQs) having structural modifications at the 6-, 7-, and 8-positions. Addition of a methoxy substituent to C-8 effected an increase in antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and a decrease in cytotoxic

Articles

The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.

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