25166-87-4 Usage
Uses
Used in Flavor and Fragrance Industry:
HEXENAL is used as a flavoring agent for its characteristic "green" vegetable odor, adding a fresh and natural scent to various food products. Its low aroma threshold values enable it to be effective even at very low concentrations.
Used in Perfumery:
In the perfumery industry, HEXENAL is used as a fragrance ingredient to provide a unique and pleasant scent to perfumes and other scented products. Its ability to be detected at low concentrations makes it an ideal choice for creating subtle and complex fragrances.
Used in Aromatherapy:
HEXENAL's distinct odor and low detection threshold make it a suitable candidate for use in aromatherapy. Its "green" vegetable scent can be used to create a calming and refreshing atmosphere, promoting relaxation and well-being.
Used in Environmental Applications:
Due to its low aroma threshold values, HEXENAL can be used in environmental applications to detect and monitor the presence of certain compounds in water and air. This can be particularly useful in monitoring pollution levels or detecting the presence of specific chemicals in various settings.
Check Digit Verification of cas no
The CAS Registry Mumber 25166-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25166-87:
(7*2)+(6*5)+(5*1)+(4*6)+(3*6)+(2*8)+(1*7)=114
114 % 10 = 4
So 25166-87-4 is a valid CAS Registry Number.
25166-87-4Relevant academic research and scientific papers
Photocatalytic One-Pot Synthesis of Homoallyl Ketones via a Norrish Type i Reaction of Cyclopentanones
Okada, Megumi,Yamada, Keiichi,Fukuyama, Takahide,Ravelli, Davide,Fagnoni, Maurizio,Ryu, Ilhyong
, p. 9365 - 9369 (2015/09/28)
A photocatalytic synthesis of homoallyl ketones was achieved via a one-pot procedure starting from a Norrish Type I reaction of cyclopentanones, followed by a decatungstate-catalyzed hydroacylation of electron-deficient olefins by the resulting 4-pentenals. The site-selective formyl H-abstraction in the second step can be explained by radical polar effects in the transition state.
Intramolecular Addition of Alkoxy Radicals. Part 4. Reductive Cyclisation of Olefinic Hydroperoxides
Taillez, Bernard,Bertrand, Michele Paula,Surzur, Jean-Marie
, p. 547 - 554 (2007/10/02)
Pent-4-enyl hydroperoxide reacts with reducing salts (FeX2, TiCl3) to afford tetrahydrofurfuryl compounds (halides or dimers) in high yield from the selective cyclisation of the pent-4-enyloxy radical.Analogous behaviour is observed for photolysis although the yields of cyclic products are lower.The photolysis of hex-5-enyl hydroperoxide does not yield cyclic products but these are observed when this hydroperoxide is reduced by FeCl2.It is suggested that metallic salts are able to complex the alkoxyl radicals thereby making them more electrophilic and hence more prone to cyclise.
