99814-65-0 Usage
Long-chain unsaturated alcohol
1-Pentadecen-3-ol is an alcohol with a long hydrocarbon chain (15 carbon atoms) and an unsaturated bond, which contributes to its unique properties.
Carbon-carbon double bond at the third position
The double bond in 1-Pentadecen-3-ol is located at the third carbon atom from the omega (end) of the molecule, which influences its chemical reactivity and physical properties.
Naturally occurring compound
1-Pentadecen-3-ol can be found in various natural sources, such as fruits, vegetables, and essential oils, indicating its widespread presence in the environment.
Use in perfumes and flavorings
Due to its pleasant aroma and taste, 1-Pentadecen-3-ol is used in the production of perfumes and flavorings, adding desirable scents and flavors to various products.
Antimicrobial properties
1-Pentadecen-3-ol has potential antimicrobial properties, which means it may be able to inhibit the growth or kill microorganisms, making it a potential candidate for use in pharmaceuticals and other applications.
Antioxidant properties
As an antioxidant, 1-Pentadecen-3-ol may help protect cells from damage caused by free radicals, which could be beneficial in the development of skincare products and other health-related applications.
Check Digit Verification of cas no
The CAS Registry Mumber 99814-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,1 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99814-65:
(7*9)+(6*9)+(5*8)+(4*1)+(3*4)+(2*6)+(1*5)=190
190 % 10 = 0
So 99814-65-0 is a valid CAS Registry Number.
99814-65-0Relevant articles and documents
Regioselective Opening of Chiral Hydroxy Epoxides: A Short Route to Muricatacin and its Diastereomer epi-Muricatacin
Saiah, Mohammed,Bessodes, Michel,Antonakis, Kostas
, p. 1597 - 1598 (1993)
The dilithioacetate opening of chiral epoxides, obtained by the Sharpless asymmetric epoxidation procedure, led regiospecifically to the corresponding hydroxy γ-lactones thus opening a short route to epimuracatacin and muricatacin.
Asymmetric synthesis of both enantiomers of a δ-lactone analogue of muricatacin
Doran, Robert,Guiry, Patrick J.
, p. 761 - 770 (2014)
The asymmetric synthesis of both enantiomers of the δ-lactone analogue of the antitumoral natural product γ-lactone muricatacin has been carried out. Initial attempts to also synthesize the natural product proved unsuccessful due to the poor reactivity of the Grignard reagent derived from 2-(bromomethyl)-1,3-dioxolane. The designed synthetic route enabled us to increase the ring size to generate the δ-lactone analogue employing Sharpless asymmetric epoxidation and ZrCl4-catalyzed intramolecular acetalization as the key steps. Georg Thieme Verlag Stuttgart.New York.
Synthesis of two possible diastereomers of reticulatain-1
Makabe, Hidefumi,Miyawaki, Aya,Takahashi, Ryoko,Hattori, Yasunao,Konno, Hiroyuki,Abe, Masato,Miyoshi, Hideto
, p. 973 - 977 (2007/10/03)
A convergent synthesis of two possible diastereomers of reticulatain-1 (1a and 1b) was accomplished. Comparison of the specific optical rotations of 1a and 1b did not allow for the strict determination of the absolute configuration. However, bis-(R)-MTPA
