21040-45-9

Basic information

• Product Name: Cinnamylcetate
• Synonyms: Cinnamylcetate;2-Propen-1-ol, 3-phenyl-, acetate, (2E)-;(E)-3-Phenyl-2-propene-1-ol acetate;(E)-3-Phenyl-2-propenyl=acetate;(E)-Cinnamyl alcohol acetate;Acetic acid (2E)-3-phenyl-2-propenyl ester;Acetic acid (E)-3-phenylallyl ester;Acetic acid (E)-cinnamyl ester
• CAS NO: 21040-45-9
• Molecular Formula: C₁₁H₁₂O₂
• Molecular Weight: 176.2118
• Mol File: 21040-45-9.mol
• Article Data: 140

Chemical Properties

• Boiling Point: 265°C (estimate)
• Flash Point: 130.496 °C
• Appearance: /
• Density: 1.0567
• Refractive Index: 1.5425 (estimate)
• CAS DataBase Reference: Cinnamylcetate(CAS DataBase Reference)
• NIST Chemistry Reference: Cinnamylcetate(21040-45-9)
• EPA Substance Registry System: Cinnamylcetate(21040-45-9)

Safety Data

• Hazardous Substances Data: 21040-45-9(Hazardous Substances Data)

Usage

Description

Cinnamylcetate, also known as trans-Cinnamyl acetate, is the only ester of cinnamic alcohol of any significant importance. It is a colorless liquid with a sweet-floral-fruity, slightly balsamic odor. Cinnamylcetate is recognized for its good fixative properties and is commonly found in cassia oil.

Uses

Used in Fragrance Industry:
Cinnamylcetate is used as a fixative and fragrance ingredient for its sweet-floral-fruity, slightly balsamic odor. It is particularly utilized in blossom compositions, such as lilac and jasmine, to enhance and prolong the scent.
Used in Flavor Industry:
In the flavor industry, Cinnamylcetate is used to create a cinnamon-fruity effect in various compositions, adding a unique taste and aroma to different products.
Please note that the provided materials do not mention any other specific applications or industries for Cinnamylcetate. The information given is limited to its use in the fragrance and flavor industries.

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 127-08-2 potassium acetate 
• 563-63-3 silver(I) acetate 
• 62296-02-0 1-(acetoxymethoxy)-3-acetoxy-1-phenylpropane 
• 7217-71-2 1-phenyl-2-propenyl acetate 
• 108-90-7 chlorobenzene 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 2466-76-4 N-Acetylimidazole 
• 75-36-5 acetyl chloride 
• 873-66-5 1-propenylbenzene 
• 546-67-8 lead(IV) tetraacetate 
• 591-87-7 Allyl acetate 
• 143-66-8 sodium tetraphenyl borate 
• 64-19-7 acetic acid 

Downstream Products

• 19950-77-7 1-acetoxy-trans-2,3-epoxy-3-phenylpropane 
• 68048-53-3 3-oxo-3-phenyl-2-phenylselenopropyl acetate 
• 95607-03-7 1-(E)-cinnamylpyrrolidine-2,5-dione 
• 7217-71-2 1-phenyl-2-propenyl acetate 
• 77134-01-1 (Z)-cinnamyl acetate 
• 22665-13-0 1-phenylallyl methyl ether 
• 24808-73-9 (E)-(3-methoxyprop-1-en-1-yl)benzene 
• 16277-67-1 (Z)-(3-methoxyprop-1-en-1-yl)benzene 
• 74120-63-1 (E)-1,4-diphenyl-1,5-hexadiene 
• 115580-35-3 (E)-4-hydroxy-6-methyl-3-(3-phenylallyl)pyran-2-one 
• 116503-99-2 3,3-dicinnamyl-6-methyl-2,4-pyrandione 
• 72651-96-8 (E)-2,2-dimethyl-5-(3-phenylallyl)-1,3-dioxane-4,6-dione 
• 121740-85-0 2,2-dimethyl-4,6-dioxo-5,5-di(3-phenyl-2-propenyl)-1,3-dioxane 
• 17480-07-8 2-[(E)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione 

Relevant articles and documents

Oxoammonium-Mediated Allylsilane–Ether Coupling Reaction

A new C(sp3)?H functionalization reaction consisting of the oxidative α-allylation of allyl- and benzyl- methyl ethers has been developed. The C?C coupling could be carried out under mild conditions thanks to the use of cheap and green oxoammonium salts. The scope of the reaction was studied over 27 examples, considering the nature of the substituents on the two coupling partners.

C–C Cross-Coupling Reactions of Organosilanes with Terminal Alkenes and Allylic Acetates Using PdII Catalyst Supported on Starch Coated Magnetic Nanoparticles

Starch coated magnetic nanoparticles supported palladium catalyst has been explored to perform C–C cross coupling reactions, such as oxidative Heck coupling and Tsuji–Trost allylic coupling using organosilicon compounds as one of the coupling partners. The biopolymer coated magnetic catalyst was very easy to recover magnetically and was efficiently recycled in the subsequent batches. All the reactions were performed in air and thus the necessity of air and moisture free reaction condition is avoided. The present protocols show wide substrate scope and good yields of the products.