149794-31-0

Basic information

• Product Name: Phosphonic acid, [(2E)-1-hydroxy-3-phenyl-2-propenyl]-, dimethyl ester
• CAS NO: 149794-31-0
• Molecular Formula: C11H15O4P
• Molecular Weight: 242.211
• Mol File: 149794-31-0.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [(2E)-1-hydroxy-3-phenyl-2-propenyl]-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [(2E)-1-hydroxy-3-phenyl-2-propenyl]-, dimethyl ester(149794-31-0)
• EPA Substance Registry System: Phosphonic acid, [(2E)-1-hydroxy-3-phenyl-2-propenyl]-, dimethyl ester(149794-31-0)

Safety Data

• Hazardous Substances Data: 149794-31-0(Hazardous Substances Data)

Upstream product

• 868-85-9 Dimethyl phosphite 
• 104-55-2 3-phenyl-propenal 
• 645-49-8 cis-stilben 
• 6329-53-9 (1-hydroxy-allyl)-phosphonic acid dimethyl ester 
• 100-42-5 styrene 
• 14371-10-9 (E)-3-phenylpropenal 
• 121-45-9 phosphorous acid trimethyl ester 
• 96-36-6 methyl phosphite 
• 75-36-5 acetyl chloride 

Downstream Products

• 74103-43-8 dimethyl (2,3-dichloro-1-hydroxy-3-phenylpropyl)phosphonate 
• 74103-46-1 dimethyl (2,3-dibromo-1-hydroxy-3-phenylpropyl)phosphonate 
• 148826-51-1 <(Z)-3-Azido-3-phenyl-2-propenyl>phosphonsaeure-dimethylester 
• 154384-68-6 (1S) dimethyl 1-<(2'R)-2'-methoxy-2'-phenylacetoxy>-3-phenyl-2E-propenyl phosphonate 
• 154460-15-8 (1S)(2E)-dimethyl [1-hydroxy-3-phenyl-2-propenyl] phosphonate 
• 162681-26-7 (R)-(+)-(1-Hydroxy-3-phenyl-2E-propenyl)phosphonic acid dimethyl ester 
• 1598391-99-1 C₁₈H₁₉FO₃ 
• 1598392-01-8 (3R,4R)-3-(4-fluorophenyl)-4-phenyltetrahydro-2H-pyran-2-one 
• 1598391-97-9 methyl (2R,3R)-5-hydroxy-2,3-diphenylpentanoate 
• 1044596-35-1 (2R,3R)-2,3-diphenylpentane-1,5-diol 
• 1598391-91-3 (2R,3R)-N¹,N⁵-diisopropyl-2,3-diphenylpentanediamide 
• 1598391-90-2 diallyl (2R,3R)-2,3-diphenylpentanedioate 
• 1598391-86-6 C₂₃H₂₂O₄ 
• 1598391-85-5 dimethyl (2R,3R)-2-(4-bromophenyl)-3-phenylpentanedioate 

Relevant articles and documents

Biocatalytic Promiscuity of Lipases in Carbon-Phosphorus Bond Formation

A promiscuous lipase-catalyzed carbon-phosphorus bond formation is presented. The developed enzymatic Pudovik-Abramov reaction of various aromatic and aliphatic aldehydes with dialkyl phosphonates provides biologically and pharmacologically relevant α-hyd

Enantioselective NHC-catalysed formal [4+2] cycloaddition of alkylaryl-ketenes with β,γ-unsaturated α-ketophosphonates

NHC-mediated enantioselective formal [4+2] cycloadditions of alkylarylketenes with γ-substituted-β,γ-unsaturated α-ketophosphonates is described. A substrate-dependent switch in diastereoselectivity was observed, with γ-aryl α-ketophosphonates providing p

Synthesis, characterization and catalytic properties of magnetic nanoparticle supported guanidine in base catalyzed synthesis of α-hydroxyphosphonates and α-acetoxyphosphonates

Magnetic nanoparticle Fe3O4-immobilized guanidine (MNPs-Guanidine) as a novel magnetically interphase nanocatalyst was synthesized and characterized. MNPs-Guanidine catalyzed the synthesis of α-hydroxyphosphonates from aldehydes and