120703-45-9 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Propanoylphenyl 2,2-dimethylpropanoate serves as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure allows it to be a valuable building block for the development of new drugs and medicinal agents.
Used in Fragrance Industry:
4-Propanoylphenyl 2,2-dimethylpropanoate is used as a fragrance ingredient due to its sweet, floral, and fruity aroma. It is a popular choice in perfumes and scented products, adding depth and complexity to the overall scent profile.
Used in Flavor Industry:
In addition to its use in fragrances, 4-Propanoylphenyl 2,2-dimethylpropanoate is also employed as a flavoring agent. Its pleasant aroma makes it suitable for enhancing the taste and smell of various food and beverage products.
Used in Antifungal and Antimicrobial Applications:
4-Propanoylphenyl 2,2-dimethylpropanoate has been studied for its potential biological and pharmacological activities, including antifungal and antimicrobial properties. Its ability to inhibit the growth of certain fungi and bacteria makes it a candidate for use in antimicrobial formulations and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 120703-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120703-45:
(8*1)+(7*2)+(6*0)+(5*7)+(4*0)+(3*3)+(2*4)+(1*5)=79
79 % 10 = 9
So 120703-45-9 is a valid CAS Registry Number.
120703-45-9Relevant academic research and scientific papers
Synthesis and structure-activity relationships of ferrocenyl tamoxifen derivatives with modifed side chains
Nguyen, Anh,Top, Siden,Pigeon, Pascal,Vessieres, Anne,Hillard, Elizabeth A.,Plamont, Marie-Aude,Huche, Michel,Rigamonti, Clara,Jaouen, Gerard
experimental part, p. 684 - 696 (2009/07/25)
We report here the synthesis and cell-proliferation properties of derivatives of the breast cancer drug tamoxifen, in which the -O(CH 2)2N-(CH3)2 side chain, responsible for the drug's antiestrogenic properties,
Organometallic analogues of tamoxifen: Effect of the amino side-chain replacement by a carbonyl ferrocenyl moiety in hydroxytamoxifen
Nguyen, Anh,Top, Siden,Vessières, Anne,Pigeon, Pascal,Huché, Michel,Hillard, Elizabeth A.,Jaouen, Gérard
, p. 1219 - 1225 (2008/02/04)
Since the widely prescribed selective estrogen receptor modulator (SERM) tamoxifen encounters growing cases of resistance in long-term treatments, alternative drugs with different therapeutic scopes have to be developed. Many investigators have modified t
