Dibenzothiophene-4-boronic acid, 98%

Name: Dibenzothiophene-4-boronic acid, 98% | 108847-20-7
Brand: J&K Chemical
SKU: JK620822_1_G
Price: 53.0 USD
Availability: OutOfStock

Cat. No JK620822_1_G

Vendor: J&K Chemical

Product Information

Product Name

Dibenzothiophene-4-boronic acid, 98%

Brand Name

J&K

Product Number

620822

CAS

108847-20-7

Molecular Formula

C12H9BO2S

Molecular Weight

228.07

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

2734329

IUPAC Name

dibenzothiophen-4-ylboronic acid

InChI Key

GOXNHPQCCUVWRO-UHFFFAOYSA-N

SMILES

B(C1=C2C(=CC=C1)C3=CC=CC=C3S2)(O)O

Properties

Melting Point

327-330

Safety Information

Precautionary Statement

P262

References

Structure–activity relationship of 2-aminodibenzothiophene pharmacophore and the discovery of aminobenzothiophenes as potent inhibitors of Mycobacterium smegmatis

Publication Name: Bioorganic & Medicinal Chemistry Letters

Publication Date: 2022-05-01

DOI: 10.1016/j.bmcl.2022.128650

Synthesis and Characterization of Triphenylethylene Derivatives with Aggregation-Induced Emission Characteristics

Publication Name: Journal of Fluorescence

Publication Date: 2011-05-21

DOI: 10.1007/s10895-011-0896-1

Transition-Metal-Catalyzed Oxidative Heck Reactions

Publication Name: Synthesis

Publication Date: 2010-04-19

DOI: 10.1055/s-0029-1218748

Of Metals

Publication Name: Science of Synthesis

Publication Date: 2001

Dibenzothiophene-4-boronic acid, 98%

Product Information

General Information

Properties

Safety Information

References

Structure–activity relationship of 2-aminodibenzothiophene pharmacophore and the discovery of aminobenzothiophenes as potent inhibitors of Mycobacterium smegmatis

Synthesis and Characterization of Triphenylethylene Derivatives with Aggregation-Induced Emission Characteristics

Transition-Metal-Catalyzed Oxidative Heck Reactions

Of Metals