146896-99-3

Basic information

• Product Name: Phosphonic acid, [(1E)-2-phenylethenyl]-, dibutyl ester
• CAS NO: 146896-99-3
• Molecular Formula: C16H25O3P
• Molecular Weight: 296.346
• Mol File: 146896-99-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [(1E)-2-phenylethenyl]-, dibutyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [(1E)-2-phenylethenyl]-, dibutyl ester(146896-99-3)
• EPA Substance Registry System: Phosphonic acid, [(1E)-2-phenylethenyl]-, dibutyl ester(146896-99-3)

Safety Data

• Hazardous Substances Data: 146896-99-3(Hazardous Substances Data)

Upstream product

• 109-47-7 dibutyl hydrogen phosphite 
• 33142-26-6 Diethyl (1-Formyl-1-phenylmethyl)phosphonate 
• 1809-19-4 dibutyl hydrogen phosphite 
• 7436-90-0 2,2-dibromostyrene 
• 100-42-5 styrene 
• 140-10-3 (E)-3-phenylacrylic acid 
• 5153-67-3 nitrostyrene 

Relevant articles and documents

Copper-mediated cross-coupling of H-phosphonates with vinyliodonium salts: A novel very mild synthesis of 2-arylvinylphosphonates

(Chemical Equation Presented) We report a novel, very mild, highly stereoselective preparation of 2-arylvinylphosphonates at room temperature that involves the copper iodide-mediated cross-coupling of H-phosphonates with vinyliodonium tetrafluoroborates.

Silver-catalyzed synthesis of 2-arylvinylphosphonates by cross-coupling of β-nitrostyrenes with: H -phosphites

An efficient protocol for stereoselective synthesis of 2-arylvinylphosphonates has been developed via AgNO3-catalyzed cross-coupling of β-nitrostyrenes with dialkyl H-phosphites under mild conditions. By losing the nitro group of β-nitrostyrene

Copper-mediated selective cross-coupling of 1,1-dibromo-1-alkenes and heteronucleophiles: Development of general routes to heterosubstituted alkynes and alkenes

Efficient and general procedures for the cross-coupling of 1,1-dibromoalkenes and N-, O-, and P-nucleophiles are reported. Fine-tuning of the reaction conditions allows for either site-selective, double, or alkynylative cross-coupling, therefore providing