61499-22-7

Usage

Uses

Used in Pharmaceutical Industry:
3-(4-Acetoxyphenyl)-1-propene is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Flavor and Fragrance Industry:
3-(4-ACETOXYPHENYL)-1-PROPENE is also used as a chemical intermediate in the production of flavoring agents and fragrances. Its sweet floral odor contributes to the creation of various scents and flavors used in the industry.
Used in Organic Synthesis:
3-(4-Acetoxyphenyl)-1-propene serves as a versatile building block in organic synthesis, enabling the production of a wide range of chemical compounds. Its reactivity and functional groups make it suitable for various chemical reactions and transformations.

InChI:InChI=1/C11H12O2/c1-3-4-10-5-7-11(8-6-10)13-9(2)12/h3,5-8H,1,4H2,2H3

Upstream product

• 501-92-8 4-(prop-2-enyl)phenol 
• 108-24-7 acetic anhydride 
• 1927-95-3 4-bromophenyl acetate 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 106-41-2 4-bromo-phenol 
• 140-67-0 Estragole 

Downstream Products

• 893403-73-1 4-(2,3-dinitrooxypropyl)phenyl acetate 
• 22805-47-6 3-(p-hydroxyphenyl)-1,2-propanediol 
• 2538-87-6 trans-p-hydroxycinnamaldehyde 
• 58505-83-2 4‐((E)-2-formylvinyl)phenyl acetate 
• 175400-09-6 4-(2-fluoro-3-iodopropyl)phenyl acetate 
• 670225-79-3 4-(2,3-epoxy-2-fluoropropyl)phenyl acetate 
• 175399-94-7 4-(2-fluoroprop-2-enyl)phenyl acetate 

Relevant academic research and scientific papers

DDQ-mediated oxidation of allylarenes: Expedient access to cinnamaldehyde-containing phenylpropanoids

Phenylpropanoid natural products containing a cinnamaldehyde motif were easily synthesized from allylarenes mediated by 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) oxidation. Representative examples described herein are five types of 4-hydroxycinnamaldehyde derivatives from monolignols biosynthesis, Boropinal C, and 7-methoxywutaifuranal from plant extracts. Especially, simple synthesis of 7-methoxywutaifuranal was exploited through selective mono-oxidation and subsequent isomerization-ring-closing-metathesis strategy.

NITRIC OXIDE DONOR NEPRILYSIN INHIBITORS

In one aspect, the invention relates to compounds having the formula: where R1, R2, R3, R7, R8, Z, X, b, and c are as defined in the specification, or a pharmaceutically acceptable salt thereof. These compounds are nitric oxide donors and have neprilysin inhibition activity. In another aspect, the invention relates to pharmaceutical compositions comprising such compounds; methods of using such compounds; and processes and intermediates for preparing such compounds.

The synthesis of phenolic propane-1, 2- and 1,3-diols as intermediates in immobilised chelatants for the borate anion

The isomeric 3-(hydroxyphenyl)propane-1, 2-diols have been synthesised from allylic precursors by epoxidation and cleavage. Several different methods have been examined for obtaining 1-(methoxyphenyl)propane-1, 3-diols. 2-(methoxyphenyl)propane-1, 3-diols and certain hydroxy analogues have been obtained from benzaldoximes converted by oxidation to methoxy- and benzyloxynitromethylbenzenes followed by hydroxymethylation with formaldehyde and catalytic hydrogenation.

NO-donor phenols: A new class of products endowed with antioxidant and vasodilator properties

The synthesis and study of the antioxidant and vasodilator properties of a new class of phenols able to release nitric oxide are described. The products were designed through a symbiotic approach using selected phenols and selected nitrooxy and furoxan NO

FeCl3-adsorbed on montmorillonite K-10: An efficient catalyst for one-pot dealkylation-acetylation of ethers

Direct conversion of ethers into acetates is achieved by treatment of ethers with acetic anhydride in the presence of FeCl3-adsorbed on montmorillonite K-10.