127707-63-5

Basic information

• Product Name: beta-Hydroxyphenethyl acetate
• CAS NO: 127707-63-5
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.203
• Mol File: 127707-63-5.mol
• Article Data: 47

Chemical Properties

• Boiling Point: 306.3°Cat760mmHg
• Flash Point: 131.4°C
• Density: 1.147g/cm³
• CAS DataBase Reference: beta-Hydroxyphenethyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: beta-Hydroxyphenethyl acetate(127707-63-5)
• EPA Substance Registry System: beta-Hydroxyphenethyl acetate(127707-63-5)

Safety Data

• Hazardous Substances Data: 127707-63-5(Hazardous Substances Data)

Upstream product

• 5381-93-1 1-hydroxy-1-phenyl-3-butanone 
• 6270-03-7 1,2-diacetoxy-1-phenyl-ethane 
• 100-42-5 styrene 
• 64-19-7 acetic acid 
• 61235-70-9 (+/-)4-phenyl-2,2-di-n-butyl-1,3,2-dioxa stannolan 
• 122-04-3 4-nitro-benzoyl chloride 
• 830-03-5 4-nitrophenol acetate 
• 75-36-5 acetyl chloride 
• 1445-45-0 Trimethyl orthoacetate 
• 93-56-1 phenylethane 1,2-diol 
• 141-78-6 ethyl acetate 
• 108-24-7 acetic anhydride 
• 2243-35-8 2-acetoxyacetophenone 
• 79-21-0 peracetic acid 

Downstream Products

• 93-56-1 phenylethane 1,2-diol 
• 6270-03-7 1,2-diacetoxy-1-phenyl-ethane 
• 104-62-1 formic acid phenethyl ester 
• 98-86-2 acetophenone 
• 2243-35-8 2-acetoxyacetophenone 
• 147256-18-6 (R)-2-hydroxy-2-phenylethyl acetate 
• 147256-19-7 (S)-2-methylcarbonyloxy-1-phenylethyl acetate 

Relevant articles and documents

Catalytic application of zinc complex of oxygen depleted 1,3-bis(pyrazole)-p-tert-butylcalix[4]arene

In this paper we have described the synthesis and coordination properties of monometallic Zinc complex of oxygen depleted bis(pyrazole)-p-tert-butylcalix[4]arene ligand. We also present the catalytic activity of the Zinc–bis(pyrazole) complex, in acetylation of alcohols and lactide polymerization.

Efficient and regioselective ring-opening of epoxides with carboxylic acid catalyzed by graphite oxide

An efficient, simple and regioselective ring-opening reaction of epoxides with various carboxylic acids under metal-free conditions is reported. The ring-opening of epoxides takes place in the presence of graphite oxide as an efficient and available catalyst to produce the corresponding 2-hydroxy monoester and 1,2-diester derivatives in good yields. Regioselective attack of the nucleo-phile, short reaction times, metal-free conditions and reusability of catalyst are among the advantages of the present protocol.

DBN-Catalyzed Regioselective Acylation of Carbohydrates and Diols in Ethyl Acetate

The 1,5-diazabicyclo[4.3.0]non-5-ene (DBN)-catalyzed regioselective acylation of carbohydrates and diols in ethyl acetate has been developed. The hydroxyl groups can be selectively acylated by the corresponding anhydride in EtOAc in the presence of a catalytic amount (as low as 0.1 equiv.) of DBN at room temperature to 40 °C. This method avoids metal catalysts and toxic solvents, which makes it comparatively green and mild, and it uses less organic base compared with other selective acylation methods. Mechanism studies indicated that DBN could catalyze the selective acylation of hydroxyl moieties through a dual H-bonding interaction.