Basic information Safety Supplier Related

(S,S)-2-Azabicyclo[3,3,0]-octane-3-carboxylic acid benzylester hydrochloride

Basic information Safety Supplier Related

(S,S)-2-Azabicyclo[3,3,0]-octane-3-carboxylic acid benzylester hydrochloride Basic information

Product Name:
(S,S)-2-Azabicyclo[3,3,0]-octane-3-carboxylic acid benzylester hydrochloride
Synonyms:
  • Cyclopenta[b]pyrrole-2-carboxylic acid, octahydro-, phenylmethyl ester, hydrochloride (1:1), (2R,3aR,6aR)-rel-
  • 2-Azabicyclo[3,3,0]-Octane-Carboxylic Acid Benzyl Ester Hydroxychloride
  • (S,S)-2-Azabicyclo[3
  • RaceMic benzyl 2-azabicyclo[3.3.0]octane-3-carboxylate hydrochloride
  • ENDO, CIS-2-AZABIC
  • (1S, 3S, 5S)-2-AZABICYCLO [3.3.0] OCTANE-3-CARBOXYLIC ACID BENZYL ESTER HYDROCHLORIDE
  • benzyl (2S,3aS,6aS)-1,2,3,3a,4,5,6,6a-octahydrocyclopenta[b]pyrrole-2-carboxylate:hydrochloride
  • (2S,6aS)-Benzyl octahydrocyclopenta[b]pyrrole-2-carboxylate hydrochloride
CAS:
93779-29-4
MF:
C15H20ClNO2
MW:
281.78
EINECS:
618-975-1
Product Categories:
  • Pharmaceutical Intermediates
  • Aromatics
  • Chiral Reagents
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrrolidines
  • INTERMEDIATESOFRAMIPRIL
  • chiral
Mol File:
93779-29-4.mol
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(S,S)-2-Azabicyclo[3,3,0]-octane-3-carboxylic acid benzylester hydrochloride Chemical Properties

Melting point:
178-182 °C(lit.)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Ethanol, Methanol (Slightly)
form 
Solid
color 
White to Off-White
Stability:
Hygroscopic
CAS DataBase Reference
93779-29-4(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3

MSDS

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(S,S)-2-Azabicyclo[3,3,0]-octane-3-carboxylic acid benzylester hydrochloride Usage And Synthesis

Chemical Properties

white to light yellow crystal powde

Uses

rel-(R,R,R)-2-Azabicyclo[3,3,0]-octane-3-carboxylic Acid Benzyl Ester Hydrochloride is an intermeidate in the synthesis of Ramipril (R111000(P)), which is an antihypertensive. Ramipril is an angiotensin converting enzyme (ACE) inhibitor, converts to the active diacid metabolite.

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