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Ethyl 2-acetyl-4-(3-methoxyphenyl)butanoate is a complex organic chemical compound with the molecular formula C14H18O4. It is a colorless to pale yellow liquid with a fruity, floral, and slightly spicy odor. ethyl 2-acetyl-4-(3-methoxyphenyl)butanoate is primarily used as a fragrance ingredient in various personal care products, such as perfumes, lotions, and soaps, due to its pleasant aroma. It is also known for its potential use in the pharmaceutical industry as a chemical intermediate. The compound is synthesized through a series of chemical reactions involving esterification and acylation processes. It is important to note that, like many chemicals, ethyl 2-acetyl-4-(3-methoxyphenyl)butanoate should be handled with care, as it may have potential health risks if not used properly.

2146-60-3

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2146-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2146-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,4 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2146-60:
(6*2)+(5*1)+(4*4)+(3*6)+(2*6)+(1*0)=63
63 % 10 = 3
So 2146-60-3 is a valid CAS Registry Number.

2146-60-3Relevant academic research and scientific papers

Hypervalent iodine(III)-induced intramolecular cyclization of α-(aryl)alkyl-β-dicarbonyl compounds: A convenient synthesis of benzannulated and spirobenzannulated compounds

Arisawa,Ramesh,Nakajima,Tohma,Kita

, p. 59 - 65 (2007/10/03)

A novel hypervalent iodine(III)-induced direct intramolecular cyclization of α-(aryl)alkyl-β-dicarbonyl compounds has been described. Both meta- and para-substituted phenol ether derivatives containing acyclic or cyclic 1,3-dicarbonyl moieties at the side chain undergo this reaction in a facile manner. The reactions afford benzannulated and spirobenzannulated compounds that are of biological importance. The reaction is found to be general, mild, and high yielding. The mechanism of the reaction has been shown to involve a cation radical intermediate.

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