73930-97-9

Basic information

• Product Name: Benzenemethanol, a-(2-phenylethenyl)-, acetate
• Synonyms: rac-1,3-diphenyl-3-acetoxyprop-1-ene;rac-1,3-diphenylprop-2-en-1-yl acetate;rac-3-acetoxy-1,3-diphenyl-1-propene;rac-1-acetoxy-1,3-diphenylprop-2-ene
• CAS NO: 73930-97-9
• Molecular Formula: C17H16O2
• Molecular Weight: 252.313
• Mol File: 73930-97-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-(2-phenylethenyl)-, acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(2-phenylethenyl)-, acetate(73930-97-9)
• EPA Substance Registry System: Benzenemethanol, a-(2-phenylethenyl)-, acetate(73930-97-9)

Safety Data

• Hazardous Substances Data: 73930-97-9(Hazardous Substances Data)

Upstream product

• 62668-02-4 (E)-1,3-diphenyl-2-propen-1-ol 
• 108-24-7 acetic anhydride 
• 4663-33-6 1,3-diphenyl-3-hydroxypropene 
• 75-36-5 acetyl chloride 
• 98-86-2 acetophenone 
• 100-52-7 benzaldehyde 
• 94-41-7 benzalacetophenone 
• 141-78-6 ethyl acetate 
• 104-55-2 3-phenyl-propenal 

Downstream Products

• 1083-30-3 dihydrochalcone 
• 95071-02-6 (R)-dimethyl 2-(1,3-diphenylallyl)malonate 
• 156901-90-5 C₂₂H₂₀O₂S 
• 156901-91-6 C₂₂H₂₀O₂S 
• 148553-11-1 (S)-3-(1',3'-di(phenyl)prop-2'-enyl)pentane-2,4-dione 
• 1252027-89-6 (R)-dimethyl 2-phenylcyclopent-3-ene-1,1-dicarboxylate 
• 1427182-98-6 C₂₃H₁₉F₃O 
• 1427182-99-7 C₂₃H₂₂O 
• 1427183-00-3 C₂₃H₂₂O 
• 95071-02-6 rac-dimethyl (1,3-diphenyl-2-propen-1-yl)malonate 

Relevant articles and documents

d-Fructose Based Spiro-Fused PHOX Ligands: Palladium Complexes and Application in Catalysis

Phosphinooxazoline (PHOX) ligands are an important class of ligands in asymmetric catalysis. Recently we reported on the synthesis of d-fructose based spiro-fused PHOX ligands. Here, we now present the application of these ligands in asymmetric alkylation

Chiral bidentate [N,S]-ferrocene ligands based on a thiazoline framework. Synthesis and use in palladium-catalyzed asymmetric allylic alkylation

An efficient method to obtain chiral 1,2-disubstituted ferrocenyl ligands has been developed. The introduction of planar chirality was accomplished by using 2-thiazoline as an ortho-directing lithiation group, and moreover, these kinds of ligands possess

SYNTHESIS OF INDENES FROM PHENYLPROPANONES USING ALUMINA CATALYST

1,3-Diphenylpropan-2-one undergoes dehydration over alumina at around 400 deg C to form 1,3-diphenylallene which cyclizes to 2-phenylindene.Since the parent ketone can be obtained under the reaction conditions from phenylacetic acid, the present reaction forms a one step syntheses of 2-phenylindene from phenylacetic acid. 3- and 4-methylphenylacetic acids also give the corresponding indenes. 1,3-Diphenylpropan-1-ones also give phenylindenes, presumably by a direct cyclodehydration reaction.