114346-31-5 | Boc-L-(4-Fmoc)aminophenylalanine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$41.00	$29.00
5g	97%	in stock	$121.00	$85.00
10g	97%	in stock	$209.00	$147.00
25g	97%	in stock	$370.00	$259.00
100g	97%	in stock	$1,178.00	$824.00

Description

• Catalog Number: AA14241
• Chemical Name: Boc-L-(4-Fmoc)aminophenylalanine
• CAS Number: 114346-31-5
• Molecular Formula: C29H30N2O6
• Molecular Weight: 502.5583
• MDL Number: MFCD00151889
• SMILES: O=C(Nc1ccc(cc1)C[C@@H](C(=O)O)NC(=O)OC(C)(C)C)OCC1c2ccccc2-c2c1cccc2

Computed Properties

• Complexity: 781
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 37
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 10
• XLogP3: 5.2

Upstream Synthesis Route

N-[(1,1-Dimethylethoxy)carbonyl]-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-L-phenylalanine is a valuable compound widely utilized in chemical synthesis processes. This compound plays a crucial role as a protecting group in peptide synthesis, where it serves to safeguard specific functional groups within a peptide molecule. By using N-[(1,1-Dimethylethoxy)carbonyl]-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-L-phenylalanine as a protecting group, chemists can selectively manipulate and modify peptide chains without affecting other parts of the molecule. This controlled reactivity is vital in the precise construction of complex peptides and proteins in organic synthesis. Moreover, the presence of the fluorenylmethoxycarbonyl (Fmoc) protecting group provides enhanced stability and facilitates efficient purification processes during peptide synthesis.