101759-72-2 | Boc-N-Me-Thr-OH

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$139.00	$97.00
1g	98%	in stock	$283.00	$198.00
5g	98%	in stock	$1,070.00	$749.00
10g	98%	in stock	$1,693.00	$1,185.00

Description

• Catalog Number: AA06798
• Chemical Name: Boc-N-Me-Thr-OH
• CAS Number: 101759-72-2
• Molecular Formula: C10H19NO5
• Molecular Weight: 233.2616
• MDL Number: MFCD02259477
• SMILES: C[C@H]([C@H](N(C(=O)OC(C)(C)C)C)C(=O)O)O

Computed Properties

• Complexity: 271
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 0.5

Upstream Synthesis Route

The compound (2S,3R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-hydroxybutanoic acid, also known as $name$, is a valuable intermediate in chemical synthesis. Its primary application lies in the field of peptide synthesis, where it serves as a key building block in the production of complex peptide structures.Specifically, (2S,3R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-hydroxybutanoic acid is commonly used as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group serves to temporarily shield the amino group, allowing for selective reactions to occur at other functional groups within the molecule without affecting the amine functionality. This protection strategy is crucial in multi-step peptide synthesis, where the precise control of reactivity and selectivity is essential.By incorporating (2S,3R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-hydroxybutanoic acid into synthetic pathways, chemists can efficiently access a wide range of peptide sequences with defined stereochemistry and functionality. Its compatibility with standard peptide coupling methodologies makes it a versatile building block for the preparation of bioactive peptides, pharmaceutical compounds, and peptide mimetics.Overall, the strategic role of (2S,3R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-hydroxybutanoic acid in chemical synthesis underscores its significance in the development of innovative peptide-based molecules with diverse biological activities and therapeutic potential.