Avibactam Impurity 3(2R,5S) Chemical Properties

InChI

InChI=1/C7H11N3O6S.Na.H/c8-6(11)5-2-1-4-3-9(5)7(12)10(4)16-17(13,14)15;;/h4-5H,1-3H2,(H2,8,11)(H,13,14,15);;/t4-,5+;;/s3

InChIKey

JKMUNBAKQJMVKG-NLZGLQCHNA-N

SMILES

C([C@H]1CC[C@@H]2N(OS(O)(=O)=O)C(=O)[N@]1C2)(=O)N.[NaH] |&1:1,4,13,r|

Avibactam Impurity 3(2R,5S) Usage And Synthesis

Uses

(2R,5S)-7-Oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide Monosodium Salt may be useful in the preparation of optically-active diazabicyclooctane derivatives as β-lactamase inhibitor and its intermediates.

Avibactam Impurity 3(2R,5S)(1383814-68-3)Related Product Information

• Avibactam INT 1
• (2S,5R)-ethyl 5-(benzyloxyaMino)piperidine-2-carboxylate
• Avibactam Impurity 15
• trans-6-benzyloxy-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid
• Carbamic acid, [2-(aminooxy)ethyl]-, 1,1-dimethylethyl ester (9CI)
• Avibactam sodium
• Avibactam Sodium Isomer
• methyl (2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylate
• tert-butyl (S)-2-((aminooxy)methyl)pyrrolidine-1-carboxylate
• Avibactam Impurity 10
• Avibatan enantiomers s, R
• tert-butyl (N-(2-(((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)oxy)ethyl)sulfamoyl)carbamate
• tert-butyl (2S)-2-((((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)oxy)methyl)pyrrolidine-1-carboxylate
• (2S,5R)-6-(benzyloxy)-7-oxo-N'-picolinoyl-1,6-diazabicyclo[3.2.1]octane-2-carbohydrazide
• (2S,5R)-N'-acetyl-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carbohydrazide
• 4-[2-(Aminooxy)ethoxy]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester
• tert-butyl ((2S)-1-(((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)oxy)propan-2-yl)carbamate
• ethyl (2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylate