33731-59-8 Usage
Description
2,5-diethyl-3,4-dihydro-2H-pyran-2-carbaldehyde is a colorless liquid chemical compound with the formula C11H16O2. It is characterized by a fruity odor and is commonly used in various industries for its pleasant aroma.
Uses
Used in Flavor and Fragrance Industry:
2,5-diethyl-3,4-dihydro-2H-pyran-2-carbaldehyde is used as a flavoring agent for its fruity scent, enhancing the taste and aroma of food and beverages.
Used in Perfume Production:
2,5-diethyl-3,4-dihydro-2H-pyran-2-carbaldehyde is utilized in the creation of perfumes and other fragrance products, where its fruity aroma contributes to the overall scent profile.
Used in Pharmaceutical Industry:
Due to its pleasant aroma, 2,5-diethyl-3,4-dihydro-2H-pyran-2-carbaldehyde has potential applications in the pharmaceutical industry, where it can be used to improve the scent of medicinal products, making them more palatable for consumers.
Used in Cosmetic Industry:
In the cosmetic industry, this compound is employed to enhance the scent of various products, such as lotions, creams, and other personal care items, providing a more appealing sensory experience for users.
Check Digit Verification of cas no
The CAS Registry Mumber 33731-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33731-59:
(7*3)+(6*3)+(5*7)+(4*3)+(3*1)+(2*5)+(1*9)=108
108 % 10 = 8
So 33731-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-3-9-5-6-10(4-2,8-11)12-7-9/h7-8H,3-6H2,1-2H3
33731-59-8Relevant articles and documents
Solvation effects in the dimerization of 2-ethylprop-2-enal
Makitra,Karpyak,Marshalok,Pal'Chikova,Pyrig
, p. 398 - 400 (2009)
Rate constants for dimerization of 2-ethylprop-2-enal in different solvents cannot be approximated using a single solvent parameter. This is possible only with the aid of multiparameter equations. Polar solvents characterized by a high cohesion energy density accelerate the process.
Synthesis and biological activity of α-alkylacrolein dimers and their derivatives
Karpiak,Marshalok,Fedevich,Avdosieva,Kovalskyi, Ya. P.
experimental part, p. 1334 - 1338 (2009/05/26)
Dimers of methacrolein and α-ethylacrolein have been obtained and undergo a Cannizzaro reaction to the corresponding pyran alcohols and sodium salts of pyran acids. Their bacteriostatic, bactericidal, and fungicidal properties have been studied.