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(1S,4S,5S,6R)-6-Carbamoyloxy-2-oxa-bicyclo[3.2.0]heptane-4-carboxylic acid benzyl ester is a complex organic compound with the molecular formula C15H17NO6. It is a derivative of bicyclo[3.2.0]heptane, featuring a carbamoyl group at the 6-position, an oxa-ring, and a benzyl ester group. (1S,4S,5S,6R)-6-Carbamoyloxy-2-oxa-bicyclo[3.2.0]heptane-4-carboxylic acid benzyl ester is characterized by its stereochemistry, with four chiral centers at positions 1, 4, 5, and 6, all having specific configurations (1S, 4S, 5S, 6R). The presence of the carbamoyl group and the ester linkage suggests potential applications in medicinal chemistry, possibly as a precursor to pharmaceuticals or as a chiral building block. Its structure and properties make it a candidate for further exploration in the synthesis of biologically active molecules.

97222-16-7

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97222-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97222-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,2 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97222-16:
(7*9)+(6*7)+(5*2)+(4*2)+(3*2)+(2*1)+(1*6)=137
137 % 10 = 7
So 97222-16-7 is a valid CAS Registry Number.

97222-16-7Upstream product

97222-16-7Downstream Products

97222-16-7Relevant academic research and scientific papers

Synthesis of a Cyclobutanone Analogue of a β-Lactam Antibiotic

Lowe, Gordon,Swain, Steven

, p. 391 - 398 (2007/10/02)

A route has been developed which allows cyclobutanone analogues of β-lactam antibiotics to be synthesized and is illustrated by the synthesis of 6-oxo-7β-phenylacetamido-2-oxabicycloheptane-4α-carboxylic acid.Although this analogue (which contained some 7α-epimer) did not show significant antibacterial activity it was a weak inhibitor of Streptomyces R61 D,D-carboxypeptidase and a time-dependent inhibitor of E.coli R-TEM and B. cereus type I β-lactamases. 7β-Chloro-6-oxo-2-oxabicycloheptane-4α-carboxylic acid also exhibited time-dependent inhibition of these β-lactamases.

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