17574-86-6 Usage
Description
(Z)-1-Acetoxy-1-heptene, a member of the allyl acetates class of organic compounds, is a colorless liquid characterized by a fruity odor. It has a molecular formula of C9H16O2 and a molecular weight of 156.22 g/mol. (Z)-1-Acetoxy-1-heptene is recognized for its applications in the flavor and fragrance industry, as well as its role in the synthesis of other chemicals and pharmaceuticals. However, it is essential to exercise caution when handling (Z)-1-Acetoxy-1-heptene due to its irritant effects on the skin, eyes, and respiratory system.
Uses
Used in Flavor and Fragrance Industry:
(Z)-1-Acetoxy-1-heptene is used as a flavoring agent and fragrance ingredient for its distinctive fruity scent. It adds a pleasant aroma to various consumer products, enhancing their appeal and sensory experience.
Used in Chemical Synthesis:
(Z)-1-Acetoxy-1-heptene serves as a key intermediate in the synthesis of other chemicals and pharmaceuticals. Its unique chemical structure allows for further reactions and modifications, contributing to the development of new and innovative products in the chemical and pharmaceutical industries.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its role in chemical synthesis, (Z)-1-Acetoxy-1-heptene may also be utilized in the development of pharmaceutical compounds. Its potential applications in this industry could include the creation of new drugs or the enhancement of existing medications.
Check Digit Verification of cas no
The CAS Registry Mumber 17574-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17574-86:
(7*1)+(6*7)+(5*5)+(4*7)+(3*4)+(2*8)+(1*6)=136
136 % 10 = 6
So 17574-86-6 is a valid CAS Registry Number.
17574-86-6Relevant articles and documents
InCl3/Me3SiBr-catalyzed direct coupling between silyl ethers and enol acetates
Onishi, Yoshiharu,Nishimoto, Yoshihiro,Yasuda, Makoto,Baba, Akio
supporting information; experimental part, p. 2762 - 2765 (2011/08/02)
A combined Lewis acid catalyst of InCl3 and Me3SiBr promoted the direct use of enol acetates in the coupling with low-reactive silyl ethers, in which functional groups including ketones and aldehydes survived. Sterically hindered silyl ethers such as ROSiEt3, ROSiPh3, ROSit-BuMe2, and ROSii-Pr3 were also applicable.
Kinetic Enzymatic Resolution of Cyclopropane Derivatives
Pietruszka, Joerg,Rieche, Anja C. M.,Wilhelm, Thorsten,Witt, Andreas
, p. 1273 - 1286 (2007/10/03)
The kinetic enzymatic resolution of various cyclopropane derivatives was systematically investigated. The study focused on synthetically useful cyclopropylmethanols (e.g., 18a/j or 19a/j) as well as some rarely investigated cyclopropanols (e.g., 24/25 or 27). The combination of enantioselective catalytic or diastereoselective synthesis of enantiomerically enriched compounds with enzymatic approaches ultimately led to the most convenient route to enantiomerically pure starting materials. Again, this was especially proven for the synthesis of cyclopropanols 18a/j and 19a/j. Key to the successful investigation was to rigorously establish an analytical tool for the analysis of enantiomeric composition of reaction mixtures.
