108593-43-7 Usage
Uses
Used in Flavor and Fragrance Industry:
Ethyl vanillate is used as a flavoring agent in food and beverages, imparting a sweet and vanilla-like taste. It is also used in perfumes and cosmetic products to provide a pleasant aroma.
Used in Pharmaceutical Industry:
Ethyl vanillate is used in the production of pharmaceuticals, where its sweet and vanilla-like odor can enhance the sensory experience of medications.
Used as a Masking Agent in Industrial Applications:
Ethyl vanillate is used as a masking agent to cover undesirable odors in various industrial applications, improving the overall sensory experience of products.
Used in Antioxidant and Antimicrobial Applications:
Ethyl vanillate has been investigated for its potential antioxidant and antimicrobial properties, making it a valuable chemical in a variety of industries. Its ability to inhibit the growth of microorganisms and reduce oxidative stress can contribute to the preservation and safety of various products.
Check Digit Verification of cas no
The CAS Registry Mumber 108593-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108593-43:
(8*1)+(7*0)+(6*8)+(5*5)+(4*9)+(3*3)+(2*4)+(1*3)=137
137 % 10 = 7
So 108593-43-7 is a valid CAS Registry Number.
108593-43-7Relevant academic research and scientific papers
Diels-Alder Reactions with 2H-Pyran-2-ones: Reactivity and Selectivity
Effenberger, Franz,Ziegler, Thomas
, p. 1339 - 1346 (2007/10/02)
2H-Pyran-2-ones 1 react with maleic anhydride (2) in a double Diels-Alder reaction to give bicyclooct-2-ene-5,6:7,8-tetracarboxylic dianhydrides 5; the syn/syn structure was established.As expected, the reactivity of 1 was increased by electron donor substituents (OR, alkyl) and diminished by electron withdrawing substituents (CO2R).The steric influence of substituents at C-6 also decrease the reactivity of 1. - Methyl propiolate (6) and phenylacetylene (9) react with 1 to form the Diels-Alder products 7 which suffer CO2 elimination to yield methyl benzoates 8 with low and biphenyls 10 with high regioselectivity, respectively.
