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L-Phenylalanine, N-(1-oxo-3-phenyl-2-propenyl)-, also known as N-(1-oxo-3-phenyl-2-propenyl)-L-phenylalanine, is a synthetic chemical compound derived from the naturally occurring amino acid L-phenylalanine. L-Phenylalanine, N-(1-oxo-3-phenyl-2-propenyl)- is characterized by the presence of a 1-oxo-3-phenyl-2-propenyl group attached to the nitrogen atom of the L-phenylalanine molecule. It is a white crystalline solid with a molecular formula of C16H15NO3 and a molecular weight of 269.30 g/mol. L-Phenylalanine, N-(1-oxo-3-phenyl-2-propenyl)- has potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other bioactive molecules. Due to its unique structure, it may exhibit different properties and reactivity compared to the parent L-phenylalanine, making it an interesting subject for further research and development.

4969-73-7

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4969-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4969-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4969-73:
(6*4)+(5*9)+(4*6)+(3*9)+(2*7)+(1*3)=137
137 % 10 = 7
So 4969-73-7 is a valid CAS Registry Number.

4969-73-7Relevant academic research and scientific papers

TASTE-MODIFYING COMPOUNDS AND USES THEREOF

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Page/Page column 14; 16, (2021/02/19)

The present disclosure generally relates to compounds useful as taste modifiers, particularly as compounds useful for enhancing umami taste, and their use in various comestible products, such as food and beverage products.

α-Ketoamides as Broad-Spectrum Inhibitors of Coronavirus and Enterovirus Replication: Structure-Based Design, Synthesis, and Activity Assessment

Zhang, Linlin,Lin, Daizong,Kusov, Yuri,Nian, Yong,Ma, Qingjun,Wang, Jiang,Von Brunn, Albrecht,Leyssen, Pieter,Lanko, Kristina,Neyts, Johan,De Wilde, Adriaan,Snijder, Eric J.,Liu, Hong,Hilgenfeld, Rolf

, p. 4562 - 4578 (2020/03/05)

The main protease of coronaviruses and the 3C protease of enteroviruses share a similar active-site architecture and a unique requirement for glutamine in the P1 position of the substrate. Because of their unique specificity and essential role in viral po

Anti-enteroviral 71(EV71) 4-iminooxazolidine-2-ketone compound as well as preparation method and application of anti-enteroviral 71(EV71) 4-iminooxazolidine-2-ketone compound

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Paragraph 0096; 0097; 0098, (2018/03/24)

The invention discloses a 4-iminooxazolidine-2-ketone enterovirus 71(EV71) 3C protease inhibitor of which the structural general formula is shown as a compound (M), each variable in the structure is defined as the specification, and the compounds are used for effectively inhibiting or stopping the replication of enterovirus 71. The invention relates to discovery and application of a compound with a structure shown as the formula (M) as well as various optical isomers of the compound, a pharmaceutically active metabolite, a medicinal salt, a solvate and a prodrug of the compound in preparation of antiviral drugs for treating hand-foot-mouth virus infection diseases and also relates to an intermediate for preparing the compound with the structure shown as the formula (M) and a synthesis method.

Pharmaceutical composition having an excellent absorption property

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, (2008/06/13)

A compound represented by the formula: STR1 wherein R1 is a hydrogen atom, a fluorine atom, a nitro group, a hydroxyl group or a hydroxyl group protected by an esterifying group; X is CO or SO2 ; --Y-- is a straight bond, a lower alkylene group, a substituted or unsubstituted vinylene group, or group having the formula --CH2 --O-- or --O--CH2 --; R2 is a substituted or unsubstituted phenyl or naphthyl group, or R2 --Y--CO is N-benzyloxycarbonylphenylalanyl, N-benzyloxycarbonyl-4-fluorophenylalanyl or N-(m-methoxycinnamoyl)-phenylalanyl group; or a non-toxic salt thereof is disclosed along with pharmaceutical compositions containing these compounds and methods of using these compositions to increase the rate of absorption of medicines.

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