119798-08-2 | Boc4-sper-co2h

Packsize	Purity	Availability	Price	Discounted Price
25mg	95%	in stock	$183.00	$128.00
100mg	95%	in stock	$345.00	$242.00
250mg	95%	in stock	$577.00	$404.00
1g	95%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AA33052
• Chemical Name: Boc4-sper-co2h
• CAS Number: 119798-08-2
• Molecular Formula: C31H58N4O10
• Molecular Weight: 646.8130200000002
• MDL Number: MFCD06656442
• SMILES: O=C(OC(C)(C)C)NCCCN(C(=O)OC(C)(C)C)CCC[C@H](N(C(=O)OC(C)(C)C)CCCNC(=O)OC(C)(C)C)C(=O)O

Computed Properties

• Complexity: 975
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 45
• Hydrogen Bond Acceptor Count: 10
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 22
• XLogP3: 4.5

Upstream Synthesis Route

The (S)-2,5-bis((tert-Butoxycarbonyl)(3-((tert-butoxycarbonyl)amino)propyl)amino)pentanoic acid, which we will refer to as $name$, is a versatile compound widely utilized in chemical synthesis. Its primary application lies in its ability to act as a chiral building block for the creation of complex molecules with specific stereochemistry. By incorporating $name$ into synthetic pathways, chemists can introduce chirality at key positions within a molecule, leading to the production of enantiomerically enriched compounds with various applications in pharmaceuticals, agrochemicals, and materials science. The tert-butoxycarbonyl (Boc) protecting groups present in the structure of $name$ enable selective manipulation of functional groups during the synthetic process, allowing for precise control over the stereochemical outcome of reactions. This feature makes $name$ a valuable tool for the efficient and selective synthesis of bioactive compounds and advanced materials with tailored properties.