495402-49-8

Basic information

• Product Name: 2-[3-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 2-[3-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 495402-49-8
• Molecular Weight: 348.366
• Mol File: 495402-49-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-[3-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[3-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(495402-49-8)
• EPA Substance Registry System: 2-[3-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(495402-49-8)

Safety Data

• Hazardous Substances Data: 495402-49-8(Hazardous Substances Data)

Upstream product

• 443776-76-9 (3‐(4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl)phenyl)methanol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 15852-73-0 (3-Bromophenyl)methanol 
• 103978-12-7 [(3-bromobenzyl)oxy](tert-butyl)dimethylsilane 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 495413-29-1 (Zn(C₄NH₂C(C₆H₃(C(CH₃)3)2)C₄NH₂C(C₆H₄CH₂OSi(CH₃)2C(CH₃)3)C₄NH₂C(C₆H₃(C(CH₃)3)2)C₄NH₂C))2 
• 866321-85-9 [5,15-bis[3,5-di(tert-butyl)phenyl]-10-[3-(([(tert-butyl)(dimethyl)silyl]oxy)methyl)phenyl]porphyrinato(2-)-κN(21),κN(22),κN(23),κN(24)]zinc(II) 
• 1428770-72-2 p-chlorophenyl tri(3′-tert-butyldimethylsilyloxymethyl[4,1′]biphenyl)silane 
• 1428770-77-7 p-bromophenyl tri(3′-tert-butyldimethylsilyloxymethyl[4,1′]biphenyl)silane 

Relevant articles and documents

Synthesis of azobenzene substituted tripod-shaped bi(p-phenylene)s. Adsorption on gold and CdS quantum-dots surfaces

We report here the synthesis of several tripod-shaped oligo(p-phenylene)s with legs composed of two phenylene units. Each leg is end-capped with a thioacetate group for adhesion to metallic surfaces. An azobenzene chromophore group is present on the functional arm of the tripod. The key step in the synthesis is the Pd-catalyzed Suzuki cross-coupling reaction of the silicon derivative core molecule with substituted phenyl moieties and azobenzene derivatives. Gold surfaces prepared by thermal evaporation and CdS quantum-dots surfaces were covered by the tripod-shaped molecules. Modified surfaces were characterized by atomic force microscopy (AFM), fluorescence, and Kelvin Probe analyses.