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(3R,5R,7S)-2-Oxo-3-(2-phenoxy-acetylamino)-1-aza-bicyclo[3.2.0]heptane-7-carboxylic acid is a complex organic compound with a molecular formula of C17H18N2O5. It features a bicyclic structure with a seven-membered ring, containing both nitrogen and oxygen atoms. The compound has three chiral centers, which are designated as R, R, and S, indicating the specific arrangement of atoms around these centers. It includes a 2-phenoxy-acetylamino group, which is an amide derived from phenol and acetic acid, and a carboxylic acid group. This chemical is known for its potential pharmaceutical applications, particularly as an inhibitor of certain enzymes, and is often studied for its effects on biological systems.

96960-48-4

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96960-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96960-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,6 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96960-48:
(7*9)+(6*6)+(5*9)+(4*6)+(3*0)+(2*4)+(1*8)=184
184 % 10 = 4
So 96960-48-4 is a valid CAS Registry Number.

96960-48-4Relevant academic research and scientific papers

γ-LACTAM ANALOGUES OF CARBAPENICILLANIC ACIDS

Baldwin, Jack E.,Adlington, Robert M.,Jones, Richard H.,Schofield, Christopher J.,Zaracostas, Constantine,Greengrass, Colin W.

, p. 4879 - 4888 (2007/10/02)

The syntheses and biological activities of the γ-lactam analogues (endo-25), (exo-25) and (26) of carbapenicillanic acids are described.The strategy employed for the synthesis of 26 effected construction of a γ-lactam onto a preformed azetidine, followed

&γ-Lactam Analogues of Carbapenicillanic Acids

Baldwin, Jack E.,Adlington, Robert M.,Jones, Richard H.,Schofield, Christopher J.,Zarocostas, Constantine,Greengrass, Colin W.

, p. 194 - 196 (2007/10/02)

The synthesis and biological evaluation of the bicyclic-4,5-γ-lactam analogues of carbapenicillanic acid are described.

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