828282-80-0

Basic information

• Product Name: 3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE)
• Synonyms: 3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE);3,3''-BIS(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE),98.0+%(GC);3,3'-Bis(trimethylsilyl)biphenyl-4,4'-diyl Ditriflate;4,4'-Bis(trifluoromethanesulfonyloxy)-3,3'-bis(trimethylsilyl)biphenyl;3,3'-Bis(trimethylsilyl)biphenyl-4,4'-diyl Ditriflate 4,4'-Bis(trifluoromethanesulfonyloxy)-3,3'-bis(trimethylsilyl)biphenyl;Methanesulfonic acid,trifluoro-, 3,3'-bis(trimethylsilyl)[1,1'-biphenyl]-4,4'-diyl ester (9CI)
• CAS NO: 828282-80-0
• Molecular Formula: C20H24F6O6S2Si2
• Molecular Weight: 594.696
• Product Categories: Si (Classes of Silicon Compounds);Si-(C)4 Compounds;Silicon Compounds (for Synthesis);Synthetic Organic Chemistry
• Mol File: 828282-80-0.mol

Chemical Properties

• Melting Point: 118 °C
• Boiling Point: 510.409°C at 760 mmHg
• Flash Point: 262.486°C
• Appearance: /
• Density: 1.38g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: 3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE)(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE)(828282-80-0)
• EPA Substance Registry System: 3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE)(828282-80-0)

Safety Data

• RIDADR: 3261
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 828282-80-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE) is used as a reagent for its mild and selective desilylation capabilities in organic reactions, facilitating the synthesis of various organic compounds and materials.
Used as a Protecting Group:
In the field of organic chemistry, 3,3''-BIS-(TRIMETHYLSILYL)BIPHENYL-4,4''-DIYL BIS(TRIFLUOROMETHANESULFONATE) serves as a protecting group for alcohols and other functional groups, allowing chemists to temporarily mask these groups during synthetic processes to prevent unwanted reactions.
Used in Research:
This chemical is often utilized by researchers and chemists for its unique properties and applications in synthetic chemistry, contributing to the advancement of chemical knowledge and the development of new compounds and materials.

InChI:InChI=1/C20H24F6O6S2Si2/c1-35(2,3)17-11-13(7-9-15(17)31-33(27,28)19(21,22)23)14-8-10-16(18(12-14)36(4,5)6)32-34(29,30)20(24,25)26/h7-12H,1-6H3