66613-51-2 Usage
Appearance
Yellow liquid A visual description of the compound's color and state (liquid).
Usage in food industry
Flavoring agent The primary function of 1-phenoxy-3-buten-2-one in the food industry, providing a specific taste or aroma to products.
Aroma
Fruity, berry-like The specific scent that 1-phenoxy-3-buten-2-one imparts to food products, reminiscent of fruits and berries.
Common applications
Baked goods, beverages, and confectionery products The types of food products in which 1-phenoxy-3-buten-2-one is typically used as a flavoring agent.
Usage in perfumery
Production of perfumes and fragrances Another application of 1-phenoxy-3-buten-2-one, in which it is used to create sweet and floral notes in scents.
Safety
Considered safe for use in food and cosmetics An assessment of the compound's safety when used within appropriate concentrations in food and cosmetic products.
Concentration limits
Appropriate concentrations The recommended limits for using 1-phenoxy-3-buten-2-one to ensure its safety and effectiveness in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 66613-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,1 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66613-51:
(7*6)+(6*6)+(5*6)+(4*1)+(3*3)+(2*5)+(1*1)=132
132 % 10 = 2
So 66613-51-2 is a valid CAS Registry Number.
66613-51-2Relevant academic research and scientific papers
REACTIONS OF α-DIAZO-KETONES-V; ETHER OXYGEN PARTICIPATION IN THE ACETOLYSIS OF α'-PHENOXY- AND α'-DIPHENYLMETHOXY-α-DIAZO-KETONES
Pusino, A.,Rosnati, V.,Solinas, C.,Vettori, U.
, p. 2259 - 2264 (2007/10/02)
The acetolysis of α-diazo-ketones 1a-d, 2 and 3a, b, c have been studied.The results obtained for 1a-d indicate that migration of the phenoxy group represents an important, alternative pathway to normal substitution only if a tertiary carbonium ion or a cyclic transition state, with the incipient positive charge located on a tertiary C atom, is involved in the reaction.Normal substitution was the only process in the case of 2 and 3a; instead, 3b and 3c gave in addition diphenylmethyl acetate and the corresponding 2-substituted-3-oxetanone, 17 and 19, produced by a cyclic mechanism involving the intermediate formation of oxonium ions 26b and 26c, respectively.
