73545-18-3 Usage
Uses
Used in Perfumery and Cosmetics Industry:
(Z)-1,1-DIETHOXY-3-HEXENE is used as a fragrance ingredient for its fruity scent, enhancing the olfactory appeal of perfumes and cosmetic products. Its natural presence in fruits and vegetables adds to its desirability as a component in these products, offering a fresh and authentic aroma.
Used in Flavoring Industry:
In the flavoring industry, (Z)-1,1-DIETHOXY-3-HEXENE is utilized as a natural flavoring compound to impart or enhance the fruity taste in food products. Its natural occurrence in edible plants makes it a preferred choice for those seeking to avoid synthetic additives.
Used in Agricultural Applications:
(Z)-1,1-DIETHOXY-3-HEXENE is studied for its potential use as a natural pesticide. It has demonstrated insecticidal activity against certain pests, suggesting that it could be a viable alternative to synthetic pesticides. This application is particularly relevant for organic farming practices where there is a preference for natural pest control methods.
While the provided materials do not detail the specific reasons for its use in each industry, the above applications are inferred from its properties as a colorless liquid with a fruity odor and its natural presence in fruits and vegetables. Further research would be necessary to confirm its efficacy and safety in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73545-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,4 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73545-18:
(7*7)+(6*3)+(5*5)+(4*4)+(3*5)+(2*1)+(1*8)=133
133 % 10 = 3
So 73545-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-4-7-8-9-10(11-5-2)12-6-3/h7-8,10H,4-6,9H2,1-3H3/b8-7-
73545-18-3Relevant articles and documents
Total synthesis of 17-isolevuglandin E4 and the structure of C22-PGF(4α)
Sha, Wei,Salomon, Robert G.
, p. 5315 - 5326 (2007/10/03)
The isolevuglandin 17-isoLGE4 (10-acetyl-11-formyl-14-hydroxynonadeca-4(Z),7(Z),12(E),16(Z)-tet raenoic acid) is a levulinaldehyde derivative that is expected to be generated during the free radical-induced oxidation of docosahexaenoic acid. A total synthesis was executed to facilitate detection and identification of 17-isoLGE4 in biological samples. Conjugate addition of a higher order vinyl cyanocuprate to a γ-alkoxy enone achieved the final carbon-carbon bond formation to complete a convergent elaboration of the 17-isoLGE4 carbon, skeleton. Attempted construction of the requisite vinyl nucleophile synthon using hydrostannylation of an alkyne was foiled by tri-n-butylstannyl radical-promoted isomerization of acis to a trans double bond. Derivatization of 17-isoLGE4 with methoxylamine under anhydrous or wet conditions generated bismethoximes of 17-isoLGE4 or the isomerized Δ11-17-isoLGE4 respectively. Analysis of the mass spectrum of a bismethoxime-pentafluorobenzyl ester-trimethylsilyl ether derivative of 17-isoLGE4 provided presumptive evidence that an incorrect structure was proposed earlier for C22-PGF(4α), the only F4-isoprostane which is produced enzymatically. We conclude that the 22-carbon analogue of PGF(2α), produced from docosahexaenoic acid by a cyclooxygenase from trout gill, does not have the same side chains as 17-isoLGE4. Furthermore, we now propose that mass spectral data reported for 'C22-PGF(4α)' support a 14-PGF(4α) structure rather than the 17-PGF(4α) structure suggested previously.
