110763-40-1 | N-Boc-l-(+)-penicillamine

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$71.00	$50.00
1g	95%	in stock	$158.00	$111.00
5g	95%	in stock	$410.00	$287.00
10g	95%	in stock	$760.00	$532.00
25g	95%	in stock	$1,505.00	$1,054.00

Description

• Catalog Number: AD42214
• Chemical Name: N-Boc-l-(+)-penicillamine
• CAS Number: 110763-40-1
• Molecular Formula: C10H19NO4S
• Molecular Weight: 249.3272
• MDL Number: MFCD02682558
• SMILES: O=C(OC(C)(C)C)N[C@@H](C(S)(C)C)C(=O)O

Computed Properties

• Complexity: 283
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 5
• XLogP3: 1.5

Upstream Synthesis Route

This product, (R)-2-((tert-Butoxycarbonyl)amino)-3-mercapto-3-methylbutanoic acid, plays a crucial role in chemical synthesis processes. Specifically, it is utilized as a key building block in peptide synthesis due to its unique structural properties. Peptides are important biomolecules that serve various functions in biological systems, making them valuable targets for research and therapeutic development. By incorporating (R)-2-((tert-Butoxycarbonyl)amino)-3-mercapto-3-methylbutanoic acid into peptide chains, chemists can efficiently control the stereochemistry and functional groups present in the final products. This compound's ability to selectively protect and modify amino acids enables the precise assembly of complex peptide structures, facilitating the synthesis of diverse peptides with specific biological activities. Additionally, the thiol functionality of this compound offers opportunities for further derivatization and crosslinking reactions, expanding its utility in the design and construction of peptide-based materials and drug candidates.