13756-18-8

Basic information

• Product Name: (1-phenyl-2-propanoyloxy-ethyl) propanoate
• Synonyms: (1-phenyl-2-propanoyloxy-ethyl) propanoate;1-Phenyl-1,2-diyl dipropanoate
• CAS NO: 13756-18-8
• Molecular Formula: C₁₄H₁₈O₄
• Molecular Weight: 250.29
• Mol File: 13756-18-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 336.2 °C at 760 mmHg
• Flash Point: 161.2 °C
• Appearance: /
• Density: 1.092 g/cm³
• Vapor Pressure: 0.000114mmHg at 25°C
• Refractive Index: 1.498
• CAS DataBase Reference: (1-phenyl-2-propanoyloxy-ethyl) propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (1-phenyl-2-propanoyloxy-ethyl) propanoate(13756-18-8)
• EPA Substance Registry System: (1-phenyl-2-propanoyloxy-ethyl) propanoate(13756-18-8)

Safety Data

• Hazardous Substances Data: 13756-18-8(Hazardous Substances Data)

Usage

Description

(1-phenyl-2-propanoyloxy-ethyl) propanoate, also known as phenylpropanoyloxyethyl propanoate, is a chemical compound with the formula C17H18O4. It is an ester that is characterized by its pleasant, fruity odor and is commonly used as a flavoring agent and fragrance ingredient in the food and cosmetic industries.

Uses

Used in Food Industry:
(1-phenyl-2-propanoyloxy-ethyl) propanoate is used as a flavoring agent for its pleasant, fruity odor, enhancing the taste and aroma of various food products.
Used in Cosmetic Industry:
(1-phenyl-2-propanoyloxy-ethyl) propanoate is used as a fragrance ingredient in the cosmetic industry, adding a pleasant scent to products such as perfumes, soaps, and other scented items.
Used in Perfume Production:
(1-phenyl-2-propanoyloxy-ethyl) propanoate is used as a key ingredient in the production of perfumes, contributing to their overall scent profile and enhancing their appeal.
Used as a Solvent:
(1-phenyl-2-propanoyloxy-ethyl) propanoate can be used as a solvent in the production of various materials, due to its ability to dissolve other substances.
Used as a Plasticizer:
(1-phenyl-2-propanoyloxy-ethyl) propanoate can also be used as a plasticizer, helping to increase the flexibility and workability of certain materials in their production process.
It is important to handle (1-phenyl-2-propanoyloxy-ethyl) propanoate with care, as it can cause skin and eye irritation in some individuals.

InChI:InChI=1/C14H18O4/c1-3-13(15)17-10-12(18-14(16)4-2)11-8-6-5-7-9-11/h5-9,12H,3-4,10H2,1-2H3

Upstream product

• 96-09-3 styrene oxide 
• 802294-64-0 propionic acid 
• 100-42-5 styrene 
• 123-62-6 propionic acid anhydride 

Downstream Products

• 16355-00-3 (R)-1-phenyl-1,2-ethanediol 
• 25779-13-9 (S)-1-phenyl-1,2-ethanediol 
• 115482-82-1 (S)-(+)-2-(propanoyloxy)-1-phenylethanol 
• 144688-34-6 (R)-(-)-1-phenylethane-1,2-diol dipropionate 
• 138877-10-8 (R)-2-hydroxy-2-phenylethyl propionate 
• 115482-85-4 Propionic acid (R)-2-hydroxy-1-phenyl-ethyl ester 
• 115482-85-4 Propionic acid (S)-2-hydroxy-1-phenyl-ethyl ester 

Relevant articles and documents

B2pin2-Mediated Palladium-Catalyzed Diacetoxylation of Aryl Alkenes with O2 as Oxygen Source and Sole Oxidant

A novel palladium-catalyzed alkene diacetoxylation with dioxygen (O2) as both the sole oxidant and oxygen source is developed, which was identified by 18O-isotope labeling studies. Control experiments suggested that bis(pinacolato)diboron (B2pin2) played a dominant intermediary role in the formation of a C-O bond. This method performed good functional group tolerance with moderate to excellent yields, which could be successfully applied to the late-stage modification of natural products. Furthermore, an atmospheric pressure of dioxygen enhances the practicability of the protocol.