94397-78-1

Basic information

• Product Name: (E)-trimethyl<2-(4-bromophenyl)ethenyl>silane
• Synonyms: (E)-trimethyl<2-(4-bromophenyl)ethenyl>silane
• CAS NO: 94397-78-1
• Molecular Weight: 255.23
• Mol File: 94397-78-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: (E)-trimethyl<2-(4-bromophenyl)ethenyl>silane(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-trimethyl<2-(4-bromophenyl)ethenyl>silane(94397-78-1)
• EPA Substance Registry System: (E)-trimethyl<2-(4-bromophenyl)ethenyl>silane(94397-78-1)

Safety Data

• Hazardous Substances Data: 94397-78-1(Hazardous Substances Data)

Upstream product

• 938-81-8 N-nitrosoacetanilide 
• 35920-23-1 acetic acid-(4-bromo-N-nitroso-anilide) 
• 589-87-7 1,4-bromoiodobenzene 
• 754-05-2 ethenyltrimethylsilane 
• 673-40-5 4-bromobenzenediazonium tetrafluoroborate 
• 766-96-1 4-bromo-1-ethynylbenzene 
• 16116-78-2 (4-bromophenyl)(trimethylsilyl)acetylene 
• 75-77-4 chloro-trimethyl-silane 
• 29955-07-5 trimethyl(diiodomethyl)silane 
• 1122-91-4 4-bromo-benzaldehyde 
• 1068-69-5 Tris(trimethylsilyl)methane 
• 1613-97-4 (E)-1-(4-bromophenyl)-N-phenylmethanimine 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 78704-49-1 1-(4-chlorophenyl)-2-trimethylsilylacetylene 

Downstream Products

• 115665-68-4 (E)-1-bromo-4-(2-bromovinyl)benzene 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 20511-04-0 (E)-4-(4-bromophenyl)but-3-ene-2-one 
• 22966-09-2 (2E)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one 

Relevant articles and documents

Asymmetric Hydrosilylation of β-Silyl Styrenes Catalyzed by a Chiral Palladium Complex

A palladium complex coordinated with a chiral SIPHOS ligand was evaluated as an efficient catalyst for asymmetric hydrosilylation of β-silyl styrenes with trichlorosilane and 23 1,2-bis(silyl) chiral compounds were produced. Good to excellent enantioselec

Structural Characterization and Unique Catalytic Performance of Silyl-Group-Substituted Geminal Dichromiomethane Complexes Stabilized with a Diamine Ligand

Stabilization by a silyl group on the methylene carbon and a diamine ligand led to the isolation of gem-dichromiomethane species. X-ray crystallography confirmed the identity of the structure of this rare example of reactive gem-dimetalloalkane species. T

One-pot synthesis of (E)-styryl ketones from styrenes

A new, efficient protocol for the highly stereoselective one-pot synthesis of (E)-styryl ketones from styrenes based on sequential ruthenium-catalyzed silylative coupling-rhodium-catalyzed desilylative acylation reactions is reported.