2293-60-9

Basic information

• Product Name: ethyl 3-hydroxy-3-phenylbutanoate
• CAS NO: 2293-60-9
• Molecular Formula: C₁₂H₁₆O₃
• Molecular Weight: 208.2536
• Mol File: 2293-60-9.mol
• Article Data: 36

Chemical Properties

• Boiling Point: 327.6°C at 760 mmHg
• Flash Point: 135.8°C
• Density: 1.095g/cm³
• Vapor Pressure: 8.08E-05mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: ethyl 3-hydroxy-3-phenylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-hydroxy-3-phenylbutanoate(2293-60-9)
• EPA Substance Registry System: ethyl 3-hydroxy-3-phenylbutanoate(2293-60-9)

Safety Data

• Hazardous Substances Data: 2293-60-9(Hazardous Substances Data)

Upstream product

• 105-36-2 ethyl bromoacetate 
• 98-86-2 acetophenone 
• 535-15-9 ethyl 1,1-dichloroacetate 
• 105-39-5 chloroacetic acid ethyl ester 
• 623-48-3 ethyl iodoacetae 
• 141-97-9 ethyl acetoacetate 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 66-25-1 hexanal 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 17510-46-2 3,3-dimethyl-2-(trimethylsilyl)oxy-1-butene 
• 7553-56-2 iodine 
• 71-43-2 benzene 
• 18295-66-4 1-ethoxy-1-(trimethylsiloxy)ethene 
• 42201-84-3 1-ethoxy-1-(tert-butyldimethylsilyloxy)ethene 

Downstream Products

• 3759-31-7 3-hydroxy-3-phenylbutanoic acid 
• 7133-68-8 3-phenylbutane-1,3-diol 
• 1504-72-9 ethyl 3-phenylbut-2-enoate 
• 118856-07-8 ethyl 3-acetoxy-3-phenylbutanoate 
• 21133-86-8 4-Ethyl-2-phenyl-hexane-2,4-diol 
• 21133-79-9 2-methyl-4-phenyl-pentane-2,4-diol 
• 28074-18-2 1,1,3-Triphenyl-butan-1,3-diol 
• 945-93-7 ethyl (E)-3-phenylbut-2-enoate 
• 54976-37-3 3-phenylbut-2-en-1-ol 
• 39171-59-0 (4-bromobut-2-en-2-yl)benzene 
• 147753-68-2 2-bromomethyl-3-methyl-3-phenyloxirane 
• 5633-64-7 ethyl 3-phenyl-3-butenoate 
• 85987-31-1 Cl₄Nb(C₆H₅C(CH₃)(O)CH₂CO₂C₂H₅) 
• 85987-32-2 Cl₃Nb(C₆H₅C(CH₃)(O)CH₂CO₂C₂H₅)2 

Relevant articles and documents

A general method for the formation of zinc enolate equivalents from iodoacetates by diisopropylzinc-iodine exchange reaction: Preparation of β-Hydroxy esters

Diisopropylzinc is found to be a highly efficient reagent for the formation of zinc enolate equivalents from various iodoacetates via iodine-Zinc exchange reaction at room temperature, affording β-Hydroxy esters in high yields by the reaction with aldehydes and ketones.

Synthesis method of beta-tertiary alcohol ester compound

The invention belongs to the technical field of medicine and organic chemical synthesis, and discloses a synthesis method of a beta-tertiary alcohol ester compound. A ketone compound and an iodo-acetate compound are used as raw materials; manganese powder

Method for preparing β - hydroxyl carbonyl compound (by machine translation)

The present invention relates to a process for preparing β - hydroxycarbonyl compounds, which mainly provides a process for the reaction, using inexpensive commercial iron powder-mediated α -halocarbonyl compounds with aldehydes/ketones, to provide the corresponding β - hydroxycarbonyl compound . the present invention relates to a method. The process is good, has wide functional group tolerance and good compatibility. (by machine translation)