73823-79-7

Basic information

• Product Name: Ethanone, 1-[4-[2-(acetyloxy)ethyl]phenyl]-
• CAS NO: 73823-79-7
• Molecular Formula: C12H14O3
• Molecular Weight: 206.241
• Mol File: 73823-79-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-[2-(acetyloxy)ethyl]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-[2-(acetyloxy)ethyl]phenyl]-(73823-79-7)
• EPA Substance Registry System: Ethanone, 1-[4-[2-(acetyloxy)ethyl]phenyl]-(73823-79-7)

Safety Data

• Hazardous Substances Data: 73823-79-7(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 103-45-7 acetic acid phenethyl ester 
• 60-12-8 2-phenylethanol 
• 94771-81-0 Acetic acid 2-[4-(1-hydroxy-ethyl)-phenyl]-ethyl ester 

Downstream Products

• 705939-53-3 C₁₄H₁₃F₃O₄ 
• 705939-70-4 C₁₄H₁₄F₂O₄ 
• 501-94-0 p-hydroxyphenethyl alcohol 
• 60037-42-5 2-(4-acetoxyphenyl)ethyl acetate 
• 1361414-32-5 4-(2-bromoacetyl)phenethyl acetate 
• 22532-49-6 4-ethylphenethylacetate 
• 705939-55-5 C₁₃H₁₁F₅O₃ 
• 705939-56-6 C₁₄H₁₆O₅ 
• 82099-82-9 Acetic acid 4-(2-methoxy-ethyl)-phenyl ester 
• 99215-52-8 4-ethoxyethylacetophenone 
• 93205-89-1 4-methoxyethylacetophenone 
• 88318-14-3 4-(2-ethoxyethyl)phenol 
• 56718-71-9 4-(2-methoxyethyl)phenol 
• 156589-19-4 (S)-2-tert-Butoxycarbonylamino-succinic acid 4-[2-(4-acetyl-2-nitro-phenyl)-ethyl] ester 

Relevant articles and documents

Synthesis method of p-hydroxyphenethyl alcohol

The invention discloses a method for synthesizing p-hydroxyphenethyl alcohol from phenethyl alcohol as a raw material. The method comprises the steps as follows: firstly, phenethyl alcohol and acid anhydride are subjected to an esterification reaction to obtain phenethyl alcohol ester; then, phenethyl alcohol ester and acid anhydride are subjected to an electrophilic substitution reaction under the action of a catalyst and a catalyst promoter to obtain 4-acryl phenethyl alcohol ester; next, 4-acryl phenethyl alcohol ester and hydrogen peroxide are subjected to a Baeyer-Villiger oxidation reaction under the action of organic acid and an oxidation catalyst to obtain 4-acyloxy phenethyl alcohol ester; finally, the 4-acyloxy phenethyl alcohol ester is subjected to a hydrolysis reaction in alkaline water to obtain p-hydroxyphenethyl alcohol. The process for synthesizing p-hydroxyphenethyl alcohol has the advantages that raw materials are widely sourced, the yield is high, the process is concise, few three wastes are produced and industrialization is easy to realize.

AMINE COMPOUND AND PHARMACEUTICAL USE THEREOF

Provided is a novel amine compound represented by the following formula (I) having a superior peripheral blood lymphocyte decreasing action and superior in the immunosuppressive action, rejection suppressive action and the like, which shows decreased side effects of, for example, bradycardia and the like, or a pharmaceutically acceptable acid addition salt thereof, or a hydrate thereof, or a solvate thereof. wherein each symbol is as defined in the specification.

Pyrazole derivatives

A compound of the formula (I): wherein R1 is hydrogen or lower alkyl; R2 is lower alkyl, etc.; R3 is lower alkoxy, etc.; R4 is hydroxy, etc.; X is O, S, etc.; Y is CH or N; Z is lower alkylene or lower alkenylene; and m is 0 or 1; or salts thereof, which are useful as a medicament.