1219200-16-4 | 3-Bromo-2-n-boc-amino-propionic acid methyl ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$252.00	$176.00
500mg	97%	in stock	$269.00	$188.00
1g	97%	in stock	$364.00	$255.00
5g	97%	in stock	$960.00	$672.00

Description

• Catalog Number: AA54770
• Chemical Name: 3-Bromo-2-n-boc-amino-propionic acid methyl ester
• CAS Number: 1219200-16-4
• Molecular Formula: C9H16BrNO4
• Molecular Weight: 282.1316399999999
• MDL Number: MFCD09261317
• SMILES: BrC[C@@H](C(=O)OC)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 237
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

Methyl 3-bromo-2-((tert-butoxycarbonyl)amino)propanoate is a versatile compound widely utilized in chemical synthesis as a key intermediate for various organic reactions. Its unique structure allows for selective functionalization at the bromine, amino, and ester functional groups, making it a valuable building block in the production of complex molecules.In organic synthesis, Methyl 3-bromo-2-((tert-butoxycarbonyl)amino)propanoate can be used for the introduction of the tert-butoxycarbonyl (Boc) protecting group on amines. This protecting group provides stability to the amine functionality, allowing selective reactions at other sites in the molecule without affecting the amine group. Additionally, the bromine atom in the compound can serve as a reactive site for diverse substitution and coupling reactions, enabling further elaboration of the molecule.Furthermore, the ester group in Methyl 3-bromo-2-((tert-butoxycarbonyl)amino)propanoate can undergo transesterification and hydrolysis reactions, offering pathways for structural modifications and functional group interconversions in chemical synthesis. Overall, the strategic placement of functional groups in this compound facilitates its utility in constructing more intricate organic molecules with controlled regioselectivity and stereochemistry.