1062586-22-4

Basic information

• Product Name: (4-(benzo[d]thiazol-2-yl)-phenyl)boronic acid
• Synonyms: (4-(benzo[d]thiazol-2-yl)-phenyl)boronic acid
• CAS NO: 1062586-22-4
• Molecular Weight: 255.105
• Mol File: 1062586-22-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (4-(benzo[d]thiazol-2-yl)-phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(benzo[d]thiazol-2-yl)-phenyl)boronic acid(1062586-22-4)
• EPA Substance Registry System: (4-(benzo[d]thiazol-2-yl)-phenyl)boronic acid(1062586-22-4)

Safety Data

• Hazardous Substances Data: 1062586-22-4(Hazardous Substances Data)

Usage

General Description

(4-(benzo[d]thiazol-2-yl)-phenyl)boronic acid is a chemical compound with the molecular formula C12H10BNO2S. It contains a boronic acid group and a benzothiazole ring, making it a valuable building block for organic synthesis and medicinal chemistry. Boronic acids are widely used in Suzuki-Miyaura coupling reactions to form carbon-carbon bonds, while benzothiazole derivatives have shown various biological activities, including antitumor, antiviral, and antibacterial properties. Therefore, this compound has potential applications in the development of pharmaceuticals and agrochemicals. Its structural and reactivity properties make it a useful tool for researchers and chemists in the field of organic chemistry and drug discovery.

Upstream product

• 121-43-7 Trimethyl borate 
• 7732-18-5 water 
• 19654-19-4 2-(4-bromophenyl)benzothiazole 
• 1122-91-4 4-bromo-benzaldehyde 
• 137-07-5 2-amino-benzenethiol 
• 6265-91-4 2-(4-chlorophenyl)benzothiazole 

Downstream Products

• 1145669-96-0 dimethyl 4-(benzo[d]thiazol-2-yl)phenylboronate 
• 1425793-79-8 7-(4,6-diphenyl-1,3,5-triazin-2-yl)-12-[4-(benzo[d]thiazol-2-yl)phenyl]-7H-dibenzo[a,g]carbazole 

Relevant articles and documents

Visible-Light-Mediated Metal-Free Synthesis of Aryl Phosphonates: Synthetic and Mechanistic Investigations

This work describes a straightforward access to a large variety of aryl phosphonates by the simple combination of diaryliodonium salts with phosphites in the presence of a base and under visible-light illumination. The reaction proceeds smoothly, tolerates various functionalities, and was applied for the synthesis of pharmaceutically relevant compounds. Mechanistic investigations, including EPR, NMR, and DFT calculations, support the postulated reaction mechanism.

THIAZOLE SYSTEM ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

The present invention relates to novel thiazole system organic electroluminescent compounds and organic light emitting diodes comprising the same. Since the thiazole system organic electroluminescent compounds according to the invention have good luminous efficiency and life property, OLED's having very good operation lifetime can be produced.