CAS 222842-99-1

Fmoc-L-4-(Otbutylcarboxymethyl)Phe-Oh

Description:

Fmoc-L-4-(Otbutylcarboxymethyl)Phe-OH, with the CAS number 222842-99-1, is a chemical compound commonly used in peptide synthesis and research. It features a phenylalanine (Phe) residue modified with a tert-butylcarboxymethyl group, which enhances its solubility and stability during synthesis. The Fmoc (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective deprotection under mild conditions. This compound is typically utilized in solid-phase peptide synthesis, where the Fmoc group can be removed to expose the amino group for subsequent coupling reactions. Its structure contributes to the overall hydrophobicity and steric bulk, influencing the folding and properties of the resulting peptides. Additionally, the tert-butylcarboxymethyl modification can provide steric hindrance, which may affect the reactivity and interaction of the peptide in biological systems. Overall, Fmoc-L-4-(Otbutylcarboxymethyl)Phe-OH is a valuable building block in the field of medicinal chemistry and peptide research.

L-Phenylalanine,4-[2-(1,1-dimethylethoxy)-2-oxoethyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

CAS: 222842-99-1

Formula: C₃₀H₃₁NO₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 501.5702

Ref: IN-DA00I4DY

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(2-(tert-butoxy)-2-oxoethyl)phenyl)propanoic acid

CAS: 222842-99-1

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(2-(tert-butoxy)-2-oxoethyl)phenyl)propanoic acid

Purity: 97%

Ref: 54-OR1041770

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(2-(tert-butoxy)-2-oxoethyl)phenyl)propanoic acid

CAS: 222842-99-1

Purity: 97%

Color and Shape: Solid

Molecular weight: 501.57901

Ref: 10-F634428