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The chemical compound "(1S)-6-benzoyloxy-1-((1S,2S)-1-benzoyloxy-2-hydroxy-2-methyl-3-(Ξ)-tetrahydropyran-2-yloxy-propyl)-5-methylene-2-oxa-7,9-diaza-bicyclo[4.2.2]decane-8,10-dione" is a complex organic molecule with a unique structure. It features a bicyclo[4.2.2]decane core, which is a type of cyclic structure consisting of two fused rings, one of which is a four-membered ring and the other a six-membered ring. The compound is characterized by the presence of two oxa bridges, indicating the presence of oxygen atoms in the ring structure. It also contains a methylene group, which is a carbon-carbon single bond, and a 5-methylene group, suggesting the presence of a double bond between carbon atoms. The molecule is adorned with several benzoyloxy groups, which are ester derivatives of benzoic acid, and a tetrahydropyran ring, a type of cyclic ether. The stereochemistry is specified with the "1S" and "2S" notations, indicating the specific three-dimensional arrangement of the atoms around the chiral centers. (1S)-6-benzoyloxy-1-((1S,2S)-1-benzoyloxy-2-hydroxy-2-methyl-3-(Ξ)-tetrahydropyran-2-yloxy-propyl)-5-methylene-2-oxa-7,9-diaza-bicyclo[4.2.2]decane-8,10-dione is likely to be of interest in the field of organic chemistry, potentially for its pharmaceutical or chemical properties, given the complexity of its structure.

71993-92-5

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71993-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71993-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,9 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71993-92:
(7*7)+(6*1)+(5*9)+(4*9)+(3*3)+(2*9)+(1*2)=165
165 % 10 = 5
So 71993-92-5 is a valid CAS Registry Number.

71993-92-5Downstream Products

71993-92-5Relevant academic research and scientific papers

Semisynthetic bicyclomycin derivatives: Preparation and antibacterial evaluation

Muller,Zak,Kump,Tosch,Wacker

, p. 689 - 705 (2007/10/21)

A number of semisynthetic bicyclomycin derivatives have been prepared by modifications at various sites of the molecule. The preparation, characterization and antimicrobial evaluation of the new compounds is described. In contrast to bicyclomycin itself,

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