1005495-74-8 | (1S,1′S,2S,2′S,3aS,3′aS,6aS,6′aS)-1,1′-(1,3-Propanediyl)bis[N-[2,6-bis(1-methylethyl)phenyl]octahydrocyclopenta[b]pyrrole-2-carboxamide 1,1′-dioxide

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	2 weeks	$137.00	$96.00
250mg	95%	2 weeks	$566.00	$396.00

Description

• Catalog Number: AE15584
• Chemical Name: (1S,1′S,2S,2′S,3aS,3′aS,6aS,6′aS)-1,1′-(1,3-Propanediyl)bis[N-[2,6-bis(1-methylethyl)phenyl]octahydrocyclopenta[b]pyrrole-2-carboxamide 1,1′-dioxide
• CAS Number: 1005495-74-8
• Molecular Formula: C43H64N4O4
• Molecular Weight: 700.9926600000003
• MDL Number: MFCD34474114
• SMILES: O=C([C@@H]1C[C@H]2[C@@H](N1(=O)CCCN1(=O)[C@H]3CCC[C@H]3C[C@H]1C(=O)Nc1c(cccc1C(C)C)C(C)C)CCC2)Nc1c(cccc1C(C)C)C(C)C

Upstream Synthesis Route

The compound (1S,1′S,2S,2′S,3aS,3′aS,6aS,6′aS)-1,1′-(1,3-Propanediyl)bis[N-[2,6-bis(1-methylethyl)phenyl]octahydrocyclopenta[b]pyrrole-2-carboxamide 1,1′-dioxide can be utilized in chemical synthesis as a versatile building block. Due to its unique structural features and functional groups, it can serve as a key intermediate in the preparation of complex organic molecules. This compound's specific stereochemistry and substituents enable it to participate in various synthetic transformations, such as coupling reactions, ring-forming reactions, and functional group manipulations. Its rigid and chiral framework also makes it a valuable tool for asymmetric synthesis, allowing for the creation of enantiomerically pure compounds. The compound's intricate molecular architecture provides opportunities for selective modifications and the construction of intricate molecular motifs, making it a valuable asset in the realm of synthetic chemistry.