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The chemical compound "(2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-acetylamino)-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid" is a complex organic molecule with a highly specific stereochemistry. It features a bicyclic ring structure with a thiazolidine ring and an azetidine ring, which are fused together. The molecule contains multiple chiral centers, indicated by the (2S,5R,6R) notation, which specifies the three-dimensional arrangement of atoms around these centers. It also includes a 7-oxo group, indicating the presence of a carbonyl group at the 7-position, and a 3,3-dimethyl group, which are both substituents on the bicyclic core. The molecule is further adorned with a phenyl group and a unique amide linkage that incorporates another phenyl ring and a meth-(E)-ylidene moiety, contributing to its overall complexity. (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-acetylamino)-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid is likely to be of interest in the field of medicinal chemistry or as a potential bioactive molecule due to its intricate structure and functional groups.

6490-08-0

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6490-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6490-08-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,9 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6490-08:
(6*6)+(5*4)+(4*9)+(3*0)+(2*0)+(1*8)=100
100 % 10 = 0
So 6490-08-0 is a valid CAS Registry Number.

6490-08-0Relevant academic research and scientific papers

Ester prodrugs of ampicillin tailored for intracellular accumulation

Fan,Paternotte,Vermander,Li,Beaujean,Scorneaux,Dumont,Osinski,Claesen,Tulkens,Sonveaux

, p. 3107 - 3112 (2007/10/03)

Seven new ester prodrugs of ampicillin with hydrolysis half-lives ranging from 65 to 308 min were synthesized. The cellular accumulation of two of them (in J774 mouse macrophages) and their activities against intracellular Staphylococcus aureus were determined in comparison with the pivaloyloxymethylester of ampicillin (pivampicillin) and ampicillin. The esters accumulated extensively and were more active than ampicillin in this in vitro system.

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