144758-83-8

Basic information

• Product Name: α-(3,5-dimethoxyphenyl)-α-(trimethylsilyloxy)acetonitrile
• Synonyms: α-(3,5-dimethoxyphenyl)-α-(trimethylsilyloxy)acetonitrile
• CAS NO: 144758-83-8
• Molecular Weight: 265.384
• Mol File: 144758-83-8.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: α-(3,5-dimethoxyphenyl)-α-(trimethylsilyloxy)acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: α-(3,5-dimethoxyphenyl)-α-(trimethylsilyloxy)acetonitrile(144758-83-8)
• EPA Substance Registry System: α-(3,5-dimethoxyphenyl)-α-(trimethylsilyloxy)acetonitrile(144758-83-8)

Safety Data

• Hazardous Substances Data: 144758-83-8(Hazardous Substances Data)

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 7311-34-4 3,5-dimethoxybenzaldehdye 

Downstream Products

• 196599-97-0 1-(3,5-Dimethoxy-phenyl)-2,2-diphenyl-2-trimethylsilanyloxy-ethanone 
• 34904-92-2 2-(3,5-dimethoxyphenyl)-2-hydroxy-1-phenylethan-1-one 
• 1424280-50-1 C₂₈H₄₆O₆Si 
• 144758-89-4 Phosphoric acid bis-(2-cyano-ethyl) ester (3,5-dimethoxy-phenyl)-(2-phenyl-[1,3]dioxolan-2-yl)-methyl ester 
• 144758-90-7 Phosphoric acid mono-[(3,5-dimethoxy-phenyl)-(2-phenyl-[1,3]dioxolan-2-yl)-methyl] ester 
• 144758-84-9 2-(α-Hydroxy-3,5-dimethoxybenzyl)-2-phenyl-1,3-dioxolane 
• 131376-66-4 1-(3,5-Dimethoxyphenyl)-2-oxo-2-phenylethyl dihydrogen phosphate 
• 34904-91-1 1-(3,5-dimethoxyphenyl)-2-oxo-2-phenylethyl acetate 
• 34911-33-6 5,7-Dimethoxy-2-phenylbenzofuran 
• 169309-14-2 Carbonic acid 1-(3,5-dimethoxy-phenyl)-2-oxo-2-phenyl-ethyl ester 4-nitro-phenyl ester 
• 188924-61-0 (3',5'-dimethoxyphenyl)phenylethane-1,2-dione 

Relevant articles and documents

Preparation method of cyanalcohol silyl ether compound

The invention discloses a preparation method of a cyanalcohol silyl ether compound. The preparation method comprises usage of a catalyst, the catalyst is a tridentate forceps-shaped ligand-stabilizedmagnesium lithium bimetallic compound. According to the

Efficient and selective aldehyde cyanosilylation catalyzed by Mg-Li bimetallic complex

A NCN-pincer ligand-based Mg-Li bimetallic complex [NCN-MgBr2][Li(THF)4] 1 has been employed as an efficient catalyst for cyanosilylation of a wide range of aldehydes with trimethylsilyl cyanide (TMSCN) at room temperature in CDClsu

Stereoselective construction of cis-decalin framework via radical domino cyclization

Steroids with A/B cis-decalin moiety and various bioactivities have attracted many synthetic chemists as target molecules and development of efficient methodology providing cis-decalins has been desired. A stereoselective domino cyclization via Mn(OAc)3 and Cu(OTf)2-mediated radical reaction was found to be effective to construct cis-decalin framework.