CAS 151213-40-0

(4aS,7aS)-Octahydro-1H-pyrrolo[3,4-b]pyridine

Formule : C₇H₁₄N₂

InChI : InChI=1S/C7H14N2/c1-2-6-4-8-5-7(6)9-3-1/h6-9H,1-5H2/t6-,7+/m0/s1

Code InChI : InChIKey=KSCPLKVBWDOSAI-NKWVEPMBSA-N

SMILES : [C@]12([C@@](CNC1)(NCCC2)[H])[H]

Synonymes :

• (1S,6S)-2,8-Diazabicyclo[4.3.0]nonane
• (1S,6S)-cis-2,8-Diazabicyclo[4.3.0]nonane
• (4AS,7aS)-Octahydro-1H-pyrrole[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-, (4aS,7aS)-
• 1H-Pyrrolo[3,4-b]pyridine, octahydro-, (4aS-cis)-
• Cis-Octahydropyrrolo[3,4-B]Pyridine
• Moxifloxacin side chain

(1S,6S)-2,8-Diazabicyclo[4.3.0]nonane

CAS : 151213-40-0

Formule : C₇H₁₄N₂

Degré de pureté : >98.0%(GC)

Couleur et forme : Colorless to Light orange to Yellow clear liquid

Masse moléculaire : 126.20

Ref: 3B-D4210

(S,S)-2,8-Diazabicyclo [4,3,0]nonane

CAS : 151213-40-0

Formule : C₇H₁₄N₂

Degré de pureté : 97%

Couleur et forme : Liquid

Masse moléculaire : 126.1995

Ref: IN-DA001N6U

(1S,6S)-2,8-Diazabicyclo[4.3.0]Nonane

CAS : 151213-40-0

(1S,6S)-2,8-Diazabicyclo[4.3.0]Nonane

Formule : C₇H₁₄N₂

Degré de pureté : 98%

Masse moléculaire : 126.2

Ref: 54-OR1007933

(4aS,7aS)-Octahydro-1H-pyrrolo[3,4-b]pyridine

CAS : 151213-40-0

Couleur et forme : Neat

Ref: 86-MM0885.15

(4S,7S)-Moxifloxacin Impurity 83

CAS : 151213-40-0

Formule : C₇H₁₄N₂

Masse moléculaire : 126.20

Ref: 4Z-M-27103

(S,S)-2,8-Diazabicyclo[4.3.0]nonane

CAS : 151213-40-0

(4aS,7aS)-Octahydro-1H-pyrrolo[3,4-b]pyridine

Formule : C₇H₁₄N₂

Degré de pureté : 97%

Masse moléculaire : 126.2

Ref: IN-DG18507

1H-Pyrrolo[3,4-b]pyridine, octahydro-, (4aS,7aS)-

CAS : 151213-40-0

Degré de pureté : 97%

Couleur et forme : Liquid

Masse moléculaire : 126.2

Ref: 10-F861928

(S,S)-2,8-Diazabicyclo[4.3.0]nonane

Produit contrôlé

CAS : 151213-40-0

Applications Moxifloxacin intermediate

Formule : C₇H₁₄N₂

Couleur et forme : Neat

Masse moléculaire : 126.2

Ref: TR-D416871

(S,S)-2,8-Diazabicyclo[4.3.0]nonane

CAS : 151213-40-0

Formule : C₇H₁₄N₂

Masse moléculaire : 126.2

Ref: ST-EA-CP-M26100

(1S,6S)-2,8-Diazabicyclo[4.3.0]nonane

CAS : 151213-40-0

(1S,6S)-2,8-Diazabicyclo[4.3.0]nonane is a chiral compound that can be made from the reaction of an organic acid with an amino alcohol. The enantiomers of this compound have shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. The synthetic process for this compound was originally developed in the 1980s by researchers at the University of Illinois. They were able to show that it was possible to make a carbonyl reduction product using imidodicarbonic acid and an organic solvent. This led to the synthesis of moxifloxacin hydrochloride, which is used as a treatment for bacterial infections such as tuberculosis or pneumonia.

Formule : C₇H₁₄N₂

Degré de pureté : Min. 95%

Couleur et forme : Colourless To Brown Liquid

Masse moléculaire : 126.2 g/mol

Ref: 3D-FD14784