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[2-(3-oxoprop-1-enyl)phenyl] acetate, also known as cinnamyl acetate, is a chemical compound characterized by its molecular formula C11H12O2. It is predominantly found in the essential oils of plants such as cinnamon, cassia, and other aromatic plants. Cinnamyl acetate is recognized for its sweet floral aroma, which is often likened to that of jasmine, and is known for its potential biological activities, including antioxidative and antimicrobial properties.

33538-94-2

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33538-94-2 Usage

Uses

Used in Fragrance and Flavor Industry:
Cinnamyl acetate is utilized as a key ingredient in the fragrance and flavor industry due to its delightful and sweet floral scent. Its aroma is reminiscent of jasmine, making it a popular choice for creating various fragrances and flavors.
Used in Perfumes:
In the perfume industry, cinnamyl acetate is employed as a fixative agent to enhance the longevity and intensity of fragrances. Its sweet floral aroma adds a pleasant and distinctive note to perfume compositions.
Used in Soaps and Cosmetics:
Cinnamyl acetate is also used in the production of soaps and cosmetics for its pleasant aroma and potential antimicrobial properties, which can contribute to the overall effectiveness and appeal of these products.
Used in Antioxidant Applications:
The antioxidative properties of cinnamyl acetate make it a potential candidate for use in various applications where protection against oxidative stress is desired, such as in the food industry to extend the shelf life of products or in the pharmaceutical industry for the development of antioxidant supplements.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, cinnamyl acetate can be used in the development of products that require antibacterial or antifungal activity, such as in the medical, food preservation, and personal care industries.
Used in Pharmaceutical Industry:
Cinnamyl acetate's potential biological activities may also make it a candidate for further research and development in the pharmaceutical industry, particularly in the areas of drug discovery and the creation of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 33538-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,3 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33538-94:
(7*3)+(6*3)+(5*5)+(4*3)+(3*8)+(2*9)+(1*4)=122
122 % 10 = 2
So 33538-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O3/c1-9(13)14-11-7-3-2-5-10(11)6-4-8-12/h2-8H,1H3

33538-94-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(Z)-3-oxoprop-1-enyl]phenyl] acetate

1.2 Other means of identification

Product number -
Other names 2-Acetoxyzimtaldehyd

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33538-94-2 SDS

33538-94-2Relevant articles and documents

Iron(III)/O2-Mediated Regioselective Oxidative Cleavage of 1-Arylbutadienes to Cinnamaldehydes

Bhowmik, Amit,Fernandes, Rodney A.

supporting information, p. 9203 - 9207 (2019/11/14)

A simple, efficient, and environmentally benevolent regioselective oxidative cleavage of 1-arylbutadienes to cinnamaldehydes mediated by iron(III) sulfate/O2 has been developed. The reaction offered good yields and excellent regioselectivity and showed good functional group tolerance (31 examples). The method is important, as few reports with limited substrate scope are available for such excellent oxidative cleavage of conjugated dienes.

Modular synthesis of (E)-cinnamaldehydes directly from allylarenes via a metal-free DDQ-mediated oxidative process

Xu, Ting-Ting,Jiang, Tao-Shan,Han, Xiao-Lan,Xu, Yuan-Hong,Qiao, Jin-Ping

, p. 5350 - 5358 (2018/08/03)

An efficient synthesis of (E)-cinnamaldehydes by a metal-free DDQ-mediated oxidative transformation of allylarenes was developed. The protocol provides a practical method to prepare diverse (E)-cinnamaldehydes with broad functional group tolerance in good to excellent yields, including easy access to natural products randainal and geranyloxy sinapyl aldehyde from plant extracts. Finally, the mechanism of a single-electron transfer process was proposed.

Synthesis and biological activity of cinnamaldehydes as angiogenesis inhibitors

Kwon, Byoung-Mog,Lee, Seung-Ho,Cho, Young-Kwon,Bok, Song-Hae,So, Seung-Ho,Youn, Mi-Ran,Chang, Soo-Ik

, p. 2473 - 2476 (2007/10/03)

A series of 2-hydroxycinnamaldehyde derivatives was synthesized for examing a structure-activity relationship for inhibition of angiogenesis. The anti-angiogenic effects of 2'-substituted cinnamaldehydes and related analogs were determined in a chick embryo chorioallantoic membrane assay system.

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