24114-57-6

Basic information

• Product Name: Phenol, 2-(3-phenyl-2-propenyl)-
• CAS NO: 24114-57-6
• Molecular Formula: C15H14O
• Molecular Weight: 210.276
• Mol File: 24114-57-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Phenol, 2-(3-phenyl-2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-(3-phenyl-2-propenyl)-(24114-57-6)
• EPA Substance Registry System: Phenol, 2-(3-phenyl-2-propenyl)-(24114-57-6)

Safety Data

• Hazardous Substances Data: 24114-57-6(Hazardous Substances Data)

Upstream product

• 139-02-6 sodium phenoxide 
• 4392-24-9 Cinnamyl bromide 
• 71-43-2 benzene 
• 108-95-2 phenol 
• 582-04-7 aurone 
• 2687-12-9 cinnamyl chloride 
• 100-52-7 benzaldehyde 
• 118-93-4 o-hydroxyacetophenone 
• 2327-99-3 1-phenylpropadiene 
• 37464-41-8 phenyl 3-phenyl-allyl ether 
• 89466-08-0 2-hydroxyphenyl boronic acid 
• 138621-80-4 1-phenyl-1-phenoxy-2-propene 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 22618-12-8 1-(o-Hydroxy-phenyl)-3-phenyl-propanon-⁽¹⁾-tosylhydrazon 

Downstream Products

• 494-12-2 flavan 
• 55568-95-1 (2R,3S,4S)-2-phenylchroman-3,4-diol 
• 1132755-87-3 (R)-3,4-dihydro-2-phenyl-2H-1-benzopyran 
• 53700-13-3 (2S,3R)-3-iodo-2-phenylchromane 
• 1350895-97-4 C₁₇H₁₈O₂ 
• 55568-98-4 (2R,3S)-2-phenylchroman-3-ol 

Relevant articles and documents

The Reduction of 2-Benzylidene-3(2H)-benzofuranones with Lithium Aluminium Hydride-Aluminium Chloride

The reduction of various 2-benzylidene-3(2H)-benzofuranones with lithium aluminium hydride-aluminium chloride in ether gave the corresponding 2-benzylbenzofurans in moderate yields.The reduction of 6-methoxy-2-(4-methoxybenzoyl)benzofuran also yielded 6-m

Pd-Catalyzed Alkene Difunctionalization Reactions of Malonate Nucleophiles: Synthesis of Substituted Cyclopentanes via Alkene Aryl-Alkylation and Akenyl-Alkylation

The Pd-catalyzed coupling of malonate nucleophiles with alkenes bearing tethered aryl or alkenyl triflates is described. These alkene difunctionalization reactions afford malonate-substituted cyclopentanes that contain fused aryl or cycloalkenyl rings. Th

Enantioselective Halo-oxy- and Halo-azacyclizations Induced by Chiral Amidophosphate Catalysts and Halo-Lewis Acids

Catalytic enantioselective halocyclization of 2-alkenylphenols and enamides have been achieved through the use of chiral amidophosphate catalysts and halo-Lewis acids. Density functional theory calculations suggested that the Lewis basicity of the catalyst played an important role in the reactivity and enantioselectivity. The resulting chiral halogenated chromans can be transformed to α-Tocopherol, α-Tocotrienol, Daedalin A and Englitazone in short steps. Furthermore, a halogenated product with an unsaturated side chain may provide polycyclic adducts under radical cyclization conditions.