117014-32-1 | Boc-asp(ofm)-oh

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$73.00	$51.00
5g	95%	in stock	$185.00	$130.00
10g	95%	in stock	$339.00	$237.00

Description

• Catalog Number: AA17354
• Chemical Name: Boc-asp(ofm)-oh
• CAS Number: 117014-32-1
• Molecular Formula: C23H25NO6
• Molecular Weight: 411.4477
• MDL Number: MFCD00076916
• SMILES: O=C(C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)OCC1c2ccccc2-c2c1cccc2

Upstream Synthesis Route

Boc-Asp(Ofm)-OH is a valuable reagent in chemical synthesis due to its ability to protect the aspartic acid residue during peptide synthesis. This compound serves as a Boc-protected aspartic acid derivative, with the Ofm (9-fluorenylmethoxycarbonyl) group providing additional protection to prevent undesired side reactions.By selectively adding the Boc-Asp(Ofm)-OH reagent to a peptide chain, chemists can control the order and direction of synthesis, ensuring the precise assembly of complex peptide structures. The Boc protecting group shields the aspartic acid residue from reacting prematurely with other molecules, allowing for stepwise peptide bond formation.Moreover, the presence of the Ofm group enhances the stability of the aspartic acid residue, particularly during acidic or basic conditions that may lead to cleavage of unprotected peptides. This protection strategy enables chemists to manipulate the peptide sequence with high fidelity, leading to the successful synthesis of bioactive peptides and pharmaceutical compounds.In summary, Boc-Asp(Ofm)-OH plays a critical role in peptide chemistry by facilitating the controlled synthesis of peptides with defined sequences and structures, thereby advancing research in drug development and biotechnology.