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((2S,3R)-2-Benzenesulfonyl-4-oxo-azetidin-3-yl)-carbamic acid benzyl ester is a complex organic compound with the molecular formula C17H15NO5S. It is a chiral molecule, featuring a 2S,3R configuration, which means that it has two chiral centers with specific spatial arrangements. The compound consists of a benzene ring attached to a sulfonyl group, which is further connected to a 4-oxo-azetidin-3-yl moiety. The carbamic acid group is esterified with a benzyl group, making it a derivative of carbamic acid. ((2S,3R)-2-Benzenesulfonyl-4-oxo-azetidin-3-yl)-carbamic acid benzyl ester is of interest in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other bioactive molecules, due to its unique structure and potential reactivity.

90497-67-9

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90497-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90497-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90497-67:
(7*9)+(6*0)+(5*4)+(4*9)+(3*7)+(2*6)+(1*7)=159
159 % 10 = 9
So 90497-67-9 is a valid CAS Registry Number.

90497-67-9Relevant academic research and scientific papers

The efficient synthesis of chiral key intermediates for monobactam antibiotics

Nishida,Shibasaki,Ikegami

, p. 765 - 768 (2007/10/02)

Chemical asymmetric syntheses of the key intermediates (4,6,8) for the synthesis of monobactam antibiotics (SQ 26776 (azthreonam, sulfazecin, and SQ 26180) are accomplished from (±)-4-phenylsulfonyl-2-azetidinone.

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