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Indole-6-boronic acid, 98%|512636|147621-18-9

Indole-6-boronic acid, 98%

Cat. No JK512636_1_G
J&K Chemical

Product Information

Product Name
Indole-6-boronic acid, 98%
Brand Name
J&K
Product Number
512636
CAS
147621-18-9
Molecular Formula
C8H8BNO2
Molecular Weight
160.97
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2763205
IUPAC Name
1H-indol-6-ylboronic acid
InChI Key
ZVMHOIWRCCZGPZ-UHFFFAOYSA-N
SMILES
B(C1=CC2=C(C=C1)C=CN2)(O)O

Properties

Melting Point
177-181

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P261
P264
P271
P280
P302+P352
P304+P340+P312
P305+P351+P338
P332+P313
P337+P313
P403+P233
P405
P501
Storage Condition
Store at 2-8℃

References

Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modification
Publication Name: Nucleic Acids Research
Publication Date: 2020-06-30
DOI: 10.1093/nar/gkaa539

Development of Inhibitors against Mycobacterium abscessus tRNA (m1G37) Methyltransferase (TrmD) Using Fragment-Based Approaches
Publication Name: Journal of Medicinal Chemistry
Publication Date: 2019-07-08
DOI: 10.1021/acs.jmedchem.9b00809

Asymmetric Suzuki-Miyaura coupling of heterocycles via Rhodium-catalysed allylic arylation of racemates
Publication Name: Nature Communications
Publication Date: 2017-06-13
DOI: 10.1038/ncomms15762

Repurposing Suzuki Coupling Reagents as a Directed Fragment Library Targeting Serine Hydrolases and Related Enzymes
Publication Name: Journal of Medicinal Chemistry
Publication Date: 2017-06-09
DOI: 10.1021/acs.jmedchem.6b01224

Arenesulfonate Electrophiles
Publication Name: Science of Synthesis
Publication Date: 2012

Indole-6-boronic acid, 98%

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