(1R,6R)-2,8-Diazabicyclo[4.3.0]nonane (Technical Grade)

CAS : 151213-42-2

Ref. TR-D417275

Informations sur le produit

• Nom: (1R,6R)-2,8-Diazabicyclo[4.3.0]nonane (Technical Grade)
• Synonymes: 1H-Pyrrolo[3,4-b]pyridine, octahydro-, (4aR,7aR)-, 1H-Pyrrolo[3,4-b]pyridine, octahydro-, (4aR-cis)-, (1R,6R)-2,8-Diazabicyclo[4.3.0]nonane, (4AR,7aR)-octahydro-1H-pyrrolo[3,4-b]pyridine, (4aS,7aS)-Octahydro-6H-Pyrrolo[3,4-b]pyridine, [(4aR,7aR)-Octahydro-6H-pyrrolo[3,4-b]pyridine, (4aS,7aS)-2,3,4,4a,5,6,7,7a-octahydro-1H-pyrrolo[3,4-b]pyridine dihydrochloride, (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine, (S,S)-2,8-Diazabicyclo[4,3,0]Nonane, (S,S)-2,8-Diazabicyclo[4,3,0]Onoane, (S,S)-2,8-Diazabicylco(4,3,0)Nonane, 1H-Pyrrolo[3,4-b]pyridine, octahydro-, (4aR,7aR)-, 1H-Pyrrolo[3,4-b]pyridine, octahydro-, (4aR-cis)-, Cis-Octahydropyrrolo[3,4-B]Pyridine, Moxifloxacin side chain, [S,S]-2,8-Diazabicyclo[4.3.0]Nonane
• CAS: 151213-42-2

Description

Applications (1R,6R)-2,8-Diazabicyclo[4.3.0]nonane is a chiral reagent used in the synthesis of pyrrolopyrimidine derivatives as dual DNA gyrase B and topoisomerase IV inhibitors and potential antibacterial agents.
References Bioorg. Med. Chem. Lett., 23, 1529 (2013);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 126.20
• Formule: C₇H₁₄N₂
• Couleur/Forme: Neat
• InChI: InChI=1S/C7H14N2/c1-2-6-4-8-5-7(6)9-3-1/h6-9H,1-5H2/t6-,7+/m1/s1
• Code InChI: InChIKey=KSCPLKVBWDOSAI-RQJHMYQMSA-N
• SMILES: C1CN[C@H]2CNC[C@H]2C1