2128285-49-2

Usage

Type of compound

boronic ester derivative

Key structural features

+ Boron atom bonded to two oxygen atoms
+ Naphtalene ring with a chlorine substituent

Uses

+ Building block in organic synthesis
Formation of carbon-carbon and carbon-heteroatom bonds
+ Reagent for Suzuki-Miyaura cross-coupling reactions
Important in medicinal chemistry and material science

Unique properties due to boron atom

+ Useful in various research and industrial applications

Upstream product

• 1034050-52-6 4-chloronaphthalen-1-yl trifluoromethanesulfonate 
• 73183-34-3 bis(pinacol)diborane 
• 604-44-4 4-chloronaphthalen-1-ol 
• 53220-82-9 1-bromo-4-chloronaphthalene 

Relevant academic research and scientific papers

Compound, electron transport material, organic electroluminescent device and display device

The present application provides a compound of general formula (I), which can be used in electron transport materials. The compound has a parent structure of benzene cyano substituted naphthalene terpyridyl, has high bond energy between atoms, has good th

SHMT INHIBITORS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

COMPOUNDS FOR BINDING PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 9 (PCSK9)

The present disclosure relates to novel compounds, methods, and compositions capable of binding to PCSK9, thereby modulating PCSK9 proprotein convertase enzyme activity. The compounds of the disclosure include compounds Formula (I).