1221439-83-3 | rel-(3a-alfa,5alfa,6a-alfa)-t-butyl 5-aminohexahydrocyclopenta[c]pyrrole-2(1h)-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$246.00	$172.00
250mg	95%	in stock	$319.00	$224.00
500mg	95%	in stock	$534.00	$374.00
1g	95%	in stock	$797.00	$558.00
5g	95%	in stock	$3,345.00	$2,341.00

Description

• Catalog Number: AI14518
• Chemical Name: rel-(3a-alfa,5alfa,6a-alfa)-t-butyl 5-aminohexahydrocyclopenta[c]pyrrole-2(1h)-carboxylate
• CAS Number: 1221439-83-3
• Molecular Formula: C12H22N2O2
• Molecular Weight: 226.31527999999997
• MDL Number: MFCD23726570
• SMILES: N[C@@H]1C[C@@H]2[C@H](C1)CN(C2)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 271
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 1

Upstream Synthesis Route

The (3aR,5s,6aS)-tert-Butyl 5-aminohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate is a versatile compound widely used in chemical synthesis due to its unique structure and properties. Commonly employed as a building block in organic reactions, this compound serves as a valuable intermediate for the synthesis of various bioactive molecules, pharmaceuticals, and organic materials.Its cyclopenta[c]pyrrole core provides a rigid and stable structure, making it an excellent scaffold for constructing complex molecules with specific stereochemical arrangements. The tert-butyl and amino groups attached to this core offer compatibility with a wide range of functional groups and reactions, enhancing its utility in diverse synthetic pathways.In chemical synthesis, (3aR,5s,6aS)-tert-Butyl 5-aminohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate can participate in key transformations such as acylation, alkylation, and cycloaddition reactions to introduce new chemical functionalities or form intricate ring systems. Its chirality and three-dimensional geometry also make it a valuable chiral building block for asymmetric synthesis, enabling the creation of enantioenriched compounds with high optical purity.Overall, the application of (3aR,5s,6aS)-tert-Butyl 5-aminohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate in chemical synthesis showcases its significance in modern organic chemistry, providing chemists with a powerful tool for constructing novel molecules and exploring new synthetic pathways.