151646-26-3 Usage
Uses
Used in Pharmaceutical Industry:
Benzenebutanoic acid, 3-Methyl-α,γ-dioxo-, ethyl est is used as an intermediate in the synthesis of pharmaceutical compounds for its potential medicinal properties. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Fragrance Industry:
In the fragrance industry, Benzenebutanoic acid, 3-Methyl-α,γ-dioxo-, ethyl est is used as a scent ingredient for its distinctive aroma profile. Its complex molecular structure contributes to the creation of unique and long-lasting fragrances, enhancing the sensory experience of various products.
Used in Flavorings Industry:
Benzenebutanoic acid, 3-Methyl-α,γ-dioxo-, ethyl est is utilized as a flavoring agent in the food and beverage industry. Its ability to impart specific taste profiles makes it a valuable component in the development of innovative and appealing flavors for a wide range of products.
Used in Organic Synthesis:
This chemical compound is also used as a building block in the synthesis of other organic compounds. Its versatile structure allows for various chemical reactions, making it a valuable precursor in the creation of new molecules with potential applications in various fields, including materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 151646-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,6,4 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 151646-26:
(8*1)+(7*5)+(6*1)+(5*6)+(4*4)+(3*6)+(2*2)+(1*6)=123
123 % 10 = 3
So 151646-26-3 is a valid CAS Registry Number.
151646-26-3Relevant academic research and scientific papers
Substituted γ-Lactones . Some Observations on the Synthesis and Reactivity of 4-Aroyl-3-hydroxy-2(5H)-furanones
Zimmer, Hans,Palmer-Sungail, R.,Ho, Douglas,Amer, Adel
, p. 161 - 167 (2007/10/02)
The reaction pathway towards formation of 4-aroyl-3-hydroxy-2(5H)-furanones 1 from the base catalysed reaction between an acetophenone, diethyl oxalate and formaldehyde was investigated.If methoxide was used as base, a transesterification was found to occur in the first step, while a side reaction, namely the retro Claisen reaction, was in competition with the desired lactone formation in the second step.The nature of the solvent and the acidic character of 1 as well as the basicity of the aminoarylene were found to have a product influence on the course of the reaction of 1 with aminoarylenes.
