40326-21-4

Basic information

• Product Name: 3-Butenenitrile, 4-phenyl-2-[(trimethylsilyl)oxy]-
• CAS NO: 40326-21-4
• Molecular Formula: C13H17NOSi
• Molecular Weight: 231.37
• Mol File: 40326-21-4.mol
• Article Data: 39

Chemical Properties

• CAS DataBase Reference: 3-Butenenitrile, 4-phenyl-2-[(trimethylsilyl)oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Butenenitrile, 4-phenyl-2-[(trimethylsilyl)oxy]-(40326-21-4)
• EPA Substance Registry System: 3-Butenenitrile, 4-phenyl-2-[(trimethylsilyl)oxy]-(40326-21-4)

Safety Data

• Hazardous Substances Data: 40326-21-4(Hazardous Substances Data)

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 7677-24-9 trimethylsilyl cyanide 
• 104-55-2 3-phenyl-propenal 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 75-77-4 chloro-trimethyl-silane 
• 2408-36-8 lithium cyanide 

Downstream Products

• 129029-61-4 2-hydroxy-4-phenylbut-3-enoic acid 
• 112068-21-0 rac-(E)-2-hydroxy-4-phenyl-3-butenoic acid methyl ester 
• 61912-03-6 2-hydroxy-4-phenyl-3-butenenitrile 
• 17431-39-9 (E)-N,N-dimethylcinnamamide 
• 103-26-4 Methyl cinnamate 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 4593-90-2 3-phenylbutyric acid 
• 100573-60-2 (E)-2-(1-Ethoxy-ethoxy)-4-phenyl-but-2-enenitrile 
• 100573-61-3 (Z)-2-(1-Ethoxy-ethoxy)-4-phenyl-but-2-enenitrile 
• 100573-05-5 2-Cyan-4-phenyl-2-(trimethylsiloxy)-3-butensaeure-ethylester 
• 100573-04-4 2-Benzyl-4-phenyl-2-(trimethylsiloxy)-3-butennitril 
• 100573-21-5 C₁₄H₁₆LiNO₂ 
• 100573-03-3 2-tert-Butyl-4-phenyl-2-(trimethylsiloxy)-3-butennitril 
• 100603-80-3 2-(2-Phenylethenyl)-2-(trimethylsiloxy)-4-pentennitril 

Relevant articles and documents

A novel yttrium-based metal-organic framework for the efficient solvent-free catalytic synthesis of cyanohydrin silyl ethers

A new porous metal-organic framework (MOF) with the chemical formula [Y5L6(OH)3(DMF)3]·5H2O (1) (where L = 3-amino-4-hydroxybenzoate) has been prepared by a solvothermal procedure. The structural char

Synthesis of magnetically recoverable imidazolium hydrogen carbonate and its application as an N-heterocyclic carbene catalyst to cyanosilylation of aldehydes and ketones

We prepared a magnetically recoverable imidazolium hydrogen carbonate by immobilizing an imidazolium hydrogen carbonate on magnetite and applied it as an N-heterocyclic carbene catalyst to the cyanosilylation of aldehydes and ketones. By employing the magnetite-supported imidazolium hydrogen carbonate as a catalyst, the cyanosilylation proceeded at 60?°C to provide the corresponding trimethylsilylated cyanohydrin in a fair chemical yield. Moreover, after the reaction, the magnetic catalyst was readily recovered by use of an external magnet and could be reused up to five times.

Strategic design and refinement of Lewis acid-base catalysis by rare-earth-metal-containing polyoxometalates

Efficient polyoxometalate (POM)-based Lewis acid-base catalysts of the rare-earth-metal-containing POMs (TBA6RE-POM, RE = Y3+, Nd3+, Eu3+, Gd3+, Tb3+, or Dy 3+) were designed and