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2-Azetidinone, 1-benzoyl-4-phenyl- is a chemical compound with the molecular formula C12H9NO2. It is a derivative of azetidinone, a four-membered cyclic amide, featuring a benzoyl group at the 1-position and a phenyl group at the 4-position. 2-Azetidinone, 1-benzoyl-4-phenyl- is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is an important intermediate in the development of certain drugs and can be used in the formation of complex molecular structures. The compound is typically synthesized through chemical reactions involving azetidinone and other organic compounds, and its properties, such as solubility and stability, can be influenced by the specific substituents and reaction conditions.

731-79-3

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731-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 731-79-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 731-79:
(5*7)+(4*3)+(3*1)+(2*7)+(1*9)=73
73 % 10 = 3
So 731-79-3 is a valid CAS Registry Number.

731-79-3Relevant academic research and scientific papers

Poly-β-peptides from functionalized β-lactam monomers and antibacterial compositions containing same

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Page/Page column 16, (2015/09/23)

Disclosed is a method of making β-polypeptides. The method includes polymerizing β-lactam-containing monomers in the presence of a base initiator and a co-initiator which is not a metal-containing molecule to yield the product β-polypeptides. Specifically disclosed are methods wherein the base initiator is potassium t-butoxide, lithium bis(trimethylsilyl)amide (LiN(TMS)2), potassium bis(trimethyl-silyl)amide, and sodium ethoxide, and the reaction is carried out in a solvent such as chloroform, dichloromethane, dimethylsulfoxide, or tetrahydrofuran.

Access to poly-β-peptides with functionalized side chains and end groups via controlled ring-opening polymerization of β-lactams

Zhang, Jihua,Kissounko, Denis A.,Lee, Sarah E.,Gellman, Samuel H.,Stahl, Shannon S.

supporting information; experimental part, p. 1589 - 1597 (2009/07/30)

Poly-β-peptides are attractive for biomedical applications because the backbone is similar enough to that of proteins for biocompatibility,but the backbone is sufficiently unnatural that these polymers evade pr oteolytic degradation. Prior investigations

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