831222-65-2

Basic information

• Product Name: Silane, (1,1-dimethylethyl)(5-ethenyl-2-methoxyphenoxy)dimethyl-
• CAS NO: 831222-65-2
• Molecular Formula: C15H24O2Si
• Molecular Weight: 264.44
• Mol File: 831222-65-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Silane, (1,1-dimethylethyl)(5-ethenyl-2-methoxyphenoxy)dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, (1,1-dimethylethyl)(5-ethenyl-2-methoxyphenoxy)dimethyl-(831222-65-2)
• EPA Substance Registry System: Silane, (1,1-dimethylethyl)(5-ethenyl-2-methoxyphenoxy)dimethyl-(831222-65-2)

Safety Data

• Hazardous Substances Data: 831222-65-2(Hazardous Substances Data)

Upstream product

• 863479-34-9 3-(tert-butyldimethylsiloxy)-4-methoxyphenylacetylene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 621-59-0 isovanillin 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 97315-18-9 p-methoxy-m-(tert-butyldimethylsilyloxy)-benzaldehyde 

Downstream Products

• 831222-66-3 5-[3-(tert-butyldimethylsilanyloxy)-4-methoxyphenyl]-3-(3,4,5-trimethoxyphenyl)-4,5-dihydroisoxazole 
• 52805-46-6 2-methoxy-5-cyanophenol 
• 1227738-17-1 2-(3-methoxy-4-(5-(2-methoxy-5-(3-(3,4,5-trimethoxyphenyl)-4,5-dihydroisoxazol-5-yl)phenoxy)pentyloxy)phenyl)-2,3-dihydroquinazolin-4(1H)-one 
• 1227738-16-0 2-(3-methoxy-4-(4-(2-methoxy-5-(3-(3,4,5-trimethoxyphenyl)-4,5-dihydroisoxazol-5-yl)phenoxy)butoxy)phenyl)-2,3-dihydroquinazolin-4(1H)-one 
• 1227738-15-9 2-(3-methoxy-4-(3-(2-methoxy-5-(3-(3,4,5-trimethoxyphenyl)-4,5-dihydroisoxazol-5-yl)phenoxy)propoxy)phenyl)-2,3-dihydroquinazolin-4(1H)-one 
• 121042-96-4 (E)-1-(3',4',5'-Trimethoxyphenyl)-2-(4''-methoxy-3''-tert-butyldimethylsiloxyphenyl)ethene 
• 621-58-9 3-hydroxy-4-methoxystyrene 
• 831222-67-4 5-[3-(tert-butyldimethylsilanyloxy)-4-methoxyphenyl]-3-(3,4,5-trimethoxyphenyl)isoxazole 

Relevant articles and documents

cis-Semihydrogenation of alkynes with amine borane complexes catalyzed by gold nanoparticles under mild conditions

Supported gold nanoparticles catalyze the semihydrogenation of alkynes to alkenes with ammonia borane or amine borane complexes in excellent yields and under mild conditions. Internal alkynes provide cis-alkenes, making this protocol an attractive alternative of the classical Lindlar's hydrogenation.

Synthesis and biological evaluation of 3,5-diaryl isoxazoline/isoxazole linked 2,3-dihydroquinazolinone hybrids as anticancer agents

A series of new 3,5-diaryl isoxazoline/isoxazole linked 2,3-dihydro quinazolinone hybrids with different linker architectures have been designed and synthesized. These compounds have been evaluated for their anticancer activity. One of the compounds 4c amongst this series has shown promising anticancer activity. Further some detailed biological assays relating to the cell cycle aspects and tubulin depolymerization activity have been examined with a view to understand the mechanism of action of this conjugate.

Total synthesis of ovalifoliolatin B, acerogenins A and C

A short and concise route for the synthesis of ovalifoliolatin B, a highly strained macrocyclic diaryl ether heptanoid natural product that also provides quick access to acerogenins A and C natural products has been reported.