1314888-30-6

Basic information

• Product Name: 1,3-bis-(tert-butoxycarbonylaminomethyl)-2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
• Synonyms: 1,3-bis-(tert-butoxycarbonylaminomethyl)-2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
• CAS NO: 1314888-30-6
• Molecular Weight: 480.385
• Mol File: 1314888-30-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-bis-(tert-butoxycarbonylaminomethyl)-2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis-(tert-butoxycarbonylaminomethyl)-2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene(1314888-30-6)
• EPA Substance Registry System: 1,3-bis-(tert-butoxycarbonylaminomethyl)-2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene(1314888-30-6)

Safety Data

• Hazardous Substances Data: 1314888-30-6(Hazardous Substances Data)

Upstream product

• 1314888-25-9 5-bromo-1,3-bis-(bromomethyl)-2-fluorobenzene 
• 99725-44-7 3,5-dimethyl-4-fluoro-1-bromobenzene 

Downstream Products

• 1314888-31-7 3,5-bis-(benzyloxycarbonylaminomethyl)-3',5'-bis-(tert-butoxycarbonylaminomethyl)-4,4'-difluorobiphenyl 

Relevant articles and documents

Substituent effects in synthetic lectins - Exploring the role of CH-π interactions in carbohydrate recognition

Contacts between aromatic surfaces and saccharide CH groups are common motifs in natural carbohydrate recognition. These CH-π interactions are modeled in "synthetic lectins" which employ oligophenyl units as apolar surfaces. Here we report the synthesis a