3239-37-0 Usage
Description
(Z)-6,10-dimethylundeca-5,9-dien-2-yl acetate is a chemical compound that belongs to the class of organic compounds known as long-chain primary alcohols. It is also classified as an oxygenated hydrocarbon, specifically an acetate ester. This versatile chemical is characterized by its floral and fruity odor, making it a valuable ingredient in various industries.
Uses
Used in Fragrance Industry:
(Z)-6,10-dimethylundeca-5,9-dien-2-yl acetate is used as a fragrance ingredient for its floral and fruity scent, enhancing the pleasant aroma of perfumes and personal care products.
Used in Pharmaceutical Industry:
(Z)-6,10-dimethylundeca-5,9-dien-2-yl acetate may be utilized as a component in the development of pharmaceutical products, potentially contributing to the creation of new medications or improving existing ones.
Used in Agricultural Industry:
This chemical may also have potential applications in the agricultural sector, possibly serving as a component in the formulation of agrochemicals or as an additive in the production of certain agricultural products.
Check Digit Verification of cas no
The CAS Registry Mumber 3239-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3239-37:
(6*3)+(5*2)+(4*3)+(3*9)+(2*3)+(1*7)=80
80 % 10 = 0
So 3239-37-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O2/c1-12(2)8-6-9-13(3)10-7-11-14(4)17-15(5)16/h8,10,14H,6-7,9,11H2,1-5H3/b13-10-
3239-37-0Relevant articles and documents
Asymmetric Cation-Olefin Monocyclization by Engineered Squalene–Hopene Cyclases
Aeberli, Natalie,Berweger, Raphael,Bornscheuer, Uwe T.,Buller, Rebecca,Dossenbach, Sandro,Eichenberger, Michael,Eichhorn, Eric,Flachsmann, Felix,Hüppi, Sean,Hortencio, Lucas,Patsch, David,Voirol, Francis,Vollenweider, Sabine
, p. 26080 - 26086 (2021/09/20)
Squalene–hopene cyclases (SHCs) have great potential for the industrial synthesis of enantiopure cyclic terpenoids. A limitation of SHC catalysis has been the enzymes’ strict (S)-enantioselectivity at the stereocenter formed after the first cyclization step. To gain enantio-complementary access to valuable monocyclic terpenoids, an SHC-wild-type library including 18 novel homologs was set up. A previously not described SHC (AciSHC) was found to synthesize small amounts of monocyclic (R)-γ-dihydroionone from (E/Z)-geranylacetone. Using enzyme and process optimization, the conversion to the desired product was increased to 79 %. Notably, analyzed AciSHC variants could finely differentiate between the geometric geranylacetone isomers: While the (Z)-isomer yielded the desired monocyclic (R)-γ-dihydroionone (>99 % ee), the (E)-isomer was converted to the (S,S)-bicyclic ether (>95 % ee). Applying the knowledge gained from the observed stereodivergent and enantioselective transformations to an additional SHC-substrate pair, access to the complementary (S)-γ-dihydroionone (>99.9 % ee) could be obtained.
