257861-23-7

Basic information

• Product Name: 3-Ethoxy-4-hydroxy-4-phenyl-1-buten
• Synonyms: 3-Ethoxy-4-hydroxy-4-phenyl-1-buten
• CAS NO: 257861-23-7
• Molecular Weight: 192.258
• Mol File: 257861-23-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Ethoxy-4-hydroxy-4-phenyl-1-buten(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Ethoxy-4-hydroxy-4-phenyl-1-buten(257861-23-7)
• EPA Substance Registry System: 3-Ethoxy-4-hydroxy-4-phenyl-1-buten(257861-23-7)

Safety Data

• Hazardous Substances Data: 257861-23-7(Hazardous Substances Data)

Upstream product

• 557-31-3 3-ethoxyprop-1-ene 
• 100-52-7 benzaldehyde 
• 3054-95-3 acrylaldehyde diethyl acetal 

Downstream Products

• 934668-01-6 2-ethoxy-1-phenylbut-3-enyl acetate 
• 934668-03-8 2-ethoxy-1-phenylbut-3-enyl 2,2,2-trifluoroacetate 
• 58509-74-3 2-iso-propyl-5-phenylfuran 
• 34721-89-6 2-methyl-5-phenyl-furan 
• 934668-11-8 1-(2-ethoxy-1-(1,1,1-trifluoroprop-2-en-2-yloxy)but-3-enyl)benzene 
• 934668-10-7 1-(2-ethoxy-1-(3-methylbut-1-en-2-yloxy)but-3-enyl)benzene 
• 934668-09-4 1-(2-ethoxy-1-(prop-1-en-2-yloxy)but-3-enyl)benzene 
• 934668-02-7 2-ethoxy-1-phenylbut-3-enyl isobutyrate 

Relevant articles and documents

A metathesis-based approach to the synthesis of furans

(Chemical Equation Presented) The enol ether-olefin ring-closing metathesis reaction has been employed to generate 2,3-dihydrofurans that are equipped with a leaving group. These substrates are at the correct oxidation state to undergo an acid-catalyzed a

Preparation and Reactions of Alkoxy Allylic Zirconium Reagents Derived from Acetals of α,β-Unsaturated Aldehydes: Remarkable Substituent Effects on Regioselectivity

Alkoxy allylic zirconium reagents, prepared from acetals of α,β-unsaturated aldehydes and "Cp2Zr", react with carbonyl compounds to give 1,2-diols or γ-hydroxy aldehyde derivatives. Key Words: zirconocene; alkoxy allylic zirconium reagent; allylic 1,2-dio