3749-34-6 Usage
Description
Ethanone, 1-(3,4-dihydro-2H-pyran-2-yl)-, also known as a ketone derivative, is a chemical compound characterized by the presence of a 3,4-dihydro-2H-pyran-2-yl group attached to the ethanone molecule. This unique structural feature endows it with potential applications in various industries, including pharmaceuticals, fragrances, and flavorings. However, due to its chemical nature, it is crucial to handle this compound with care to avoid potential health hazards.
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(3,4-dihydro-2H-pyran-2-yl)is used as an intermediate in the synthesis of various pharmaceutical compounds for its unique structural properties that can be exploited in drug design and development. Its ability to form specific interactions with biological targets makes it a valuable component in creating novel therapeutic agents.
Used in Fragrance Industry:
In the fragrance industry, Ethanone, 1-(3,4-dihydro-2H-pyran-2-yl)is used as a component in creating complex and unique scents. Its distinct chemical structure contributes to the overall olfactory profile of a fragrance, providing a nuanced and sophisticated aroma.
Used in Flavoring Industry:
Ethanone, 1-(3,4-dihydro-2H-pyran-2-yl)is also utilized in the flavoring industry to enhance or create specific taste profiles in food and beverages. Its unique chemical properties allow it to contribute to the overall flavor experience, adding depth and complexity to various products.
Check Digit Verification of cas no
The CAS Registry Mumber 3749-34-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3749-34:
(6*3)+(5*7)+(4*4)+(3*9)+(2*3)+(1*4)=106
106 % 10 = 6
So 3749-34-6 is a valid CAS Registry Number.
3749-34-6Relevant articles and documents
Recrossing and dynamic matching effects on selectivity in a diels-alder reaction
Wang, Zhihong,Hirschi, Jennifer S.,Singleton, Daniel A.
, p. 9156 - 9159 (2009)
Up and down the hill: The products from the hetero-Diels-Alder reaction of acrolein with methyl vinyl ketone arise from a single transition state (see scheme) and trajectory studies accurately predict the selectivity. In an extension of the dynamic matchi
