20125-81-9 Usage
Description
(E)-Oct-2-en-4-ol, also known as 2-Octen-4-ol, is a chemical compound characterized by its sweet, mushroom-like odor. It is a volatile organic compound that is naturally present in a variety of fruits, vegetables, and fungi, and is valued for its distinctive scent and antimicrobial properties.
Uses
Used in the Food and Beverage Industry:
(E)-Oct-2-en-4-ol is used as a flavoring agent for its sweet, mushroom-like aroma, enhancing the taste and smell of various products in the food and beverage sector.
Used in the Perfume and Fragrance Industry:
(E)-Oct-2-en-4-ol is utilized as a key ingredient in the production of perfumes and fragrances, where its unique scent contributes to the creation of complex and appealing scents.
Used in Cleaning and Sanitizing Products:
Due to its antimicrobial properties, (E)-Oct-2-en-4-ol is employed in some cleaning and sanitizing products to help eliminate harmful microorganisms and maintain a hygienic environment.
Used as a Precursor in Organic Synthesis:
(E)-Oct-2-en-4-ol also serves as a valuable precursor in the synthesis of other organic compounds, contributing to the development of new materials and products across various industries.
Safety Note:
It is important to handle (E)-Oct-2-en-4-ol with care, as it can cause skin and eye irritation when exposed to high concentrations. Proper safety measures should be taken during its use and storage to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 20125-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,2 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20125-81:
(7*2)+(6*0)+(5*1)+(4*2)+(3*5)+(2*8)+(1*1)=59
59 % 10 = 9
So 20125-81-9 is a valid CAS Registry Number.
20125-81-9Relevant articles and documents
PERFUME SYSTEM FOR PERFUMED CONSUMER PRODUCT
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Page/Page column 24; 25, (2021/10/30)
The present invention relates to a perfume system comprising a core-shell microcapsule A, optionally, a core-shell microcapsule B, and optionally, a free perfume oil, wherein the core of the core-shell microcapsule A and/or the free perfume oil comprises a 2-oxoacetate derivative of formula (I) as well as a perfumed consumer product comprising the same and methods and uses of the same for enhancing, conferring, increasing and/or modifying the fragrance properties and/or the fragrance intensity of perfumed consumer products.
Suzuki-Miyaura cross-couplings of secondary allylic boronic esters
Glasspoole, Ben W.,Ghozati, Kazem,Moir, Jonathon W.,Crudden, Cathleen M.
supporting information; experimental part, p. 1230 - 1232 (2012/02/15)
Palladium-catalyzed cross-coupling reactions of secondary allylic boronic esters with iodoarenes were demonstrated under the conditions previously described for the coupling of benzylic substrates. The regioselectivity of the process was largely dictated by the pattern of olefin substitution. The Royal Society of Chemistry 2012.
Synthesis of vinyl 1,2-diketones
Habel, Lothar W.,De Keersmaecker, Sigrid,Wahlen, Joos,Jacobs, Pierre A.,De Vos, Dirk E.
, p. 4057 - 4059 (2007/10/03)
A new route is outlined for preparation of vinyl 1,2-diketones via a three-step sequence. First, allylic alcohols are photooxidized by 1O2 to hydroperoxides, which are reduced to vinyl 1,2-diols. These vinyl 1,2-diols are oxidized to vinyl 1,2-diketones with oxoammonium salts, which are prepared in situ from organic nitroxyl radicals. The new route is short, avoids the use of protecting groups, and is generally applicable to obtain aliphatic or aromatic vinyl 1,2-diketones.
