1576-85-8 Usage
Description
4-PENTEN-1-YL ACETATE, also known as an acetate ester of pent-4-en-1-ol, is a clear yellow liquid with a fruity aroma. It is a chemical compound derived from the esterification of pent-4-en-1-ol with acetic acid, resulting in a unique combination of properties that make it suitable for various applications across different industries.
Uses
Used in Flavor and Fragrance Industry:
4-PENTEN-1-YL ACETATE is used as a flavoring agent for its fruity aroma, adding a pleasant and refreshing scent to various food products and beverages. Its ability to mimic natural fruit flavors makes it a popular choice in the creation of artificial flavors.
Used in Perfumery:
In the perfumery industry, 4-PENTEN-1-YL ACETATE is used as a fragrance ingredient to provide a fresh and fruity note to perfumes and colognes. Its distinct aroma can enhance the overall scent profile of a fragrance, making it a valuable addition to the perfumer's palette.
Used in Cosmetics:
4-PENTEN-1-YL ACETATE is also utilized in the cosmetics industry, where it serves as a key ingredient in the formulation of personal care products such as lotions, creams, and shampoos. Its fruity aroma and clear yellow liquid form contribute to the sensory experience of these products, making them more appealing to consumers.
Used in the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 4-PENTEN-1-YL ACETATE may also find applications in the pharmaceutical industry, potentially as a solvent or carrier for various drugs due to its chemical properties and compatibility with other substances.
Check Digit Verification of cas no
The CAS Registry Mumber 1576-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1576-85:
(6*1)+(5*5)+(4*7)+(3*6)+(2*8)+(1*5)=98
98 % 10 = 8
So 1576-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-3-4-5-6-9-7(2)8/h3H,1,4-6H2,2H3
1576-85-8Relevant articles and documents
Synthesis of the ABC Substructure of Brevenal by Sequential exo-Mode Oxacyclizations of Acyclic Polyene Precursors
Hurtak, Jessica A.,McDonald, Frank E.
, p. 6036 - 6039 (2017)
Exploratory studies on the sequential exo-mode oxacyclizations of acyclic polyene precursors have provided a substantial substructure of brevenal, including the fused tricyclic polyether with stereochemical patterns consistent with the AB and BC ring fusions. The synthesis of acyclic substrates featured two variations of Cr(II)/Ni(II) couplings for preparing 1,1-disubstituted allylic alcohols. A sequence of iodine-promoted cycloetherification, base-promoted intramolecular conjugate addition, and mercury-promoted cycloetherification produced the tricyclic substructure.
A Pd-Catalyzed [4 + 2] Annulation Approach to Fluorinated N-Heterocycles
García-Vázquez, Víctor,Hoteite, Larry,Lakeland, Christopher P.,Watson, David W.,Harrity, Joseph P. A.
supporting information, p. 2811 - 2815 (2021/05/05)
3-Fluoro- and trifluoromethylthio-piperidines represent important building blocks for discovery chemistry. We report a simple and efficient method to access analogs of these compounds that are armed with rich functionality allowing them to be chemoselectively derivatized with high diastereocontrol.
POLYMERIZATION OF OLEFINS
-
, (2008/06/13)
Olefins containing selected functional groups such as silyl, ether and alkenyl, and often containing a blocking group, may be copolymerized with unsubstituted olefins such as ethylene and propylene in the presence of certain coordination compounds of nickel or palladium. The resulting polymers are useful as molding resins, elastomers, in adhesives and for films.
