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(1S,6S)-2,8-diazabicyclo[4.3.0]nonane is a bicyclic compound with a unique molecular structure, characterized by its stereochemistry with the 1S and 6S configurations. It is a versatile molecule with potential applications in various fields due to its chemical properties and reactivity.

169533-56-6

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169533-56-6 Usage

Uses

Used in Pharmaceutical Industry:
(1S,6S)-2,8-diazabicyclo[4.3.0]nonane is used as a synthetic intermediate for the one-pot preparation of 7-heterocyclyl-substituted 3-quinolonecarboxylic acid-derivative antibiotics. Its application in this field is due to its ability to facilitate the synthesis of complex antibiotic structures, which are essential for treating bacterial infections.
Used in Antibacterial Development:
(1S,6S)-2,8-diazabicyclo[4.3.0]nonane is used as an impurity in the development of Moxifloxacin (M745000), a fluorinated quinolone antibacterial. The presence of (1S,6S)-2,8-diazabicyclo[4.3.0]nonane in the synthesis process may affect the purity and efficacy of the final product, making it an important consideration in the development and production of effective antibacterial agents.

Check Digit Verification of cas no

The CAS Registry Mumber 169533-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169533-56:
(8*1)+(7*6)+(6*9)+(5*5)+(4*3)+(3*3)+(2*5)+(1*6)=166
166 % 10 = 6
So 169533-56-6 is a valid CAS Registry Number.

169533-56-6Relevant academic research and scientific papers

A novel synthesis of (4aS,7aS)-Octahydro-1H-pyrrolo[3,4-b]pyridine:An intermediate of Moxifloxacin Hydrochloride

Reddy, G. Prashanth,Bandichhor, Rakeshwar

, p. 8701 - 8707 (2013)

A novel synthesis of (4aS, 7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine (1) is demonstrated alongwith recovery and reuse of chiral auxiliary naproxen. Further to this alternative stereoselective reduction procedures on 6-benzyl-5H- pyrrolo[3,4-b]pyridine-5,7(6H)-dione 3 enabling the desired chirality in the nonane 1 is demonstrated.

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