330645-19-7 Usage
Uses
Used in Research Applications:
3-(P-BENZYLOXYPHENYL)-DL-BETA-ALANINE is used as a research chemical for [application reason]. This could include its use in the synthesis of other compounds, as a reagent in chemical reactions, or for studying its properties and potential applications in various fields of chemistry and biochemistry.
Used in Pharmaceutical Industry:
3-(P-BENZYLOXYPHENYL)-DL-BETA-ALANINE is used as a building block or intermediate in the synthesis of pharmaceutical compounds for [application reason]. Its unique structure and functional groups may contribute to the development of new drugs or drug candidates with specific therapeutic properties.
Used in Biochemical Research:
3-(P-BENZYLOXYPHENYL)-DL-BETA-ALANINE is used as a biochemical research tool for [application reason]. It may be employed in studies investigating enzyme mechanisms, protein interactions, or other biological processes where its unique structure and functional groups can provide insights into molecular recognition and binding events.
Check Digit Verification of cas no
The CAS Registry Mumber 330645-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,6,4 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 330645-19:
(8*3)+(7*3)+(6*0)+(5*6)+(4*4)+(3*5)+(2*1)+(1*9)=117
117 % 10 = 7
So 330645-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO3/c17-15(10-16(18)19)13-6-8-14(9-7-13)20-11-12-4-2-1-3-5-12/h1-9,15H,10-11,17H2,(H,18,19)
330645-19-7Relevant academic research and scientific papers
Scaffold hopping via ANCHOR.QUERY: β-lactams as potent p53-MDM2 antagonists
Shaabani,Neochoritis,Twarda-Clapa,Musielak,Holak,D?mling
supporting information, p. 1046 - 1052 (2017/07/12)
Using the pharmacophore-based virtual screening platform ANCHOR.QUERY, we morphed our recently described Ugi-4CR scaffold towards a β-lactam scaffold with potent p53-MDM2 antagonizing activities. 2D-HSQC and FP measurements confirm potent MDM2 binding. Molecular modeling studies were used to understand the observed SAR in the β-lactam series.
Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium
Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov
, p. 1113 - 1124 (2007/10/03)
The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.
