121154-36-7

Basic information

• Product Name: Cyclopenta[b]pyrrole-2-carboxylic acid, octahydro-, [2S-(2alpha,3aalpha,6aalpha)]- (9CI)
• Synonyms: Cyclopenta[b]pyrrole-2-carboxylic acid, octahydro-, [2S-(2alpha,3aalpha,6aalpha)]- (9CI)
• CAS NO: 121154-36-7
• Molecular Formula: C₈H₁₃NO₂
• Molecular Weight: 155.19432
• Product Categories: CARBOXYLICACID;PYRROLE
• Mol File: 121154-36-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclopenta[b]pyrrole-2-carboxylic acid, octahydro-, [2S-(2alpha,3aalpha,6aalpha)]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopenta[b]pyrrole-2-carboxylic acid, octahydro-, [2S-(2alpha,3aalpha,6aalpha)]- (9CI)(121154-36-7)
• EPA Substance Registry System: Cyclopenta[b]pyrrole-2-carboxylic acid, octahydro-, [2S-(2alpha,3aalpha,6aalpha)]- (9CI)(121154-36-7)

Safety Data

• Hazardous Substances Data: 121154-36-7(Hazardous Substances Data)

Upstream product

• 87623-98-1 (2R,3aS,6aR)-1-Acetyl-octahydro-cyclopenta[b]pyrrole-2-carbonitrile 
• 89226-36-8 N-[(1S,2R)-2-(2-Chloro-2-cyano-ethyl)-cyclopentyl]-acetamide 
• 142-29-0 cyclopentene 
• 87623-98-1 (2S,3aR,6aR)-1-Acetyl-octahydro-cyclopenta[b]pyrrole-2-carbonitrile 
• 121080-49-7 benzyl N-benzyloxycarbonyl-(1R,3S,5R)-2-azabicyclo<3.3.0>octane-3-carboxylate 
• 147406-85-7 (2R,6R,8S,12S)-1-aza-10-oxo-12-phenyltricyclo<6.4.0^1,8.0^2,6>dodecan-9-one 
• 121080-48-6 (S)-Hexahydro-cyclopenta[b]pyrrole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 

Downstream Products

• 125419-12-7 methyl N-methyl-(1SR,3SR,5SR)-2-azabicyclo<3.3.0>octane-3-carboxylate 
• 93779-31-8 benzyl (1R^*,3R^*,5R^*)-2-azabicyclo<3.3.0>octane-3-carboxylate 

Relevant articles and documents

Enantiocontrolled construction of bicyclic proline derivatives via one-pot generation and intramolecular trapping of chiral stabilised azomethine ylids

Aldehydes possessing unsaturation at C-5 or C-6 condense with nylmorpholin-2-one (1), generating chiral stabilised azomethine ylids which undergo concommitant diastereospecific intramolecular 3+2 dipolar cycloaddition to furnish adducts (2), (4), and (5)

Enantioselective synthesis of 1S, 3S, 5S- and 1R, 3S, 5R-2-Azabicyclo[3.3.0]octane-3-carboxylic acid starting from L-serine

(1S, 3S, 5S)- and (1R, 3S, 5R)-2-Azabicyclo[3.3.0]octane-3-carboxylic acid have been synthesized by intramolecular radical cyclisation of methyl 2-(S)-[N-benzyloxycarbonyl-N-(2-cyclopenten-l-yl)amino]-3-iodopropionate and subsequent reactions.