Fmoc-ACHPA, or 9-fluorenylmethoxycarbonyl-α-amino-cyclohexylpropionic acid, is a chemical compound commonly used in peptide synthesis and drug development. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The compound contains an α-amino acid structure, which is essential for forming peptide bonds. Its cyclohexyl side chain contributes to the hydrophobic character, influencing the compound's solubility and interaction with biological membranes. Fmoc-ACHPA is particularly noted for its role in enhancing the stability and bioactivity of peptides, making it valuable in medicinal chemistry. The compound is typically handled under standard laboratory conditions, and safety precautions should be observed due to potential irritant properties. Overall, Fmoc-ACHPA serves as a versatile building block in the synthesis of complex peptide structures, facilitating advancements in therapeutic applications.

Fmoc-ACHPA

130597-31-8: Fmoc-ACHPA, or 9-fluorenylmethoxycarbonyl-α-amino-cyclohexylpropionic acid, is a chemical compound commonly used in peptide synthesis and drug development. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The compound contains an α-amino acid structure, which is essential for forming peptide bonds. Its cyclohexyl side chain contributes to the hydrophobic character, influencing the compound's solubility and interaction with biological membranes. Fmoc-ACHPA is particularly noted for its role in enhancing the stability and bioactivity of peptides, making it valuable in medicinal chemistry. The compound is typically handled under standard laboratory conditions, and safety precautions should be observed due to potential irritant properties. Overall, Fmoc-ACHPA serves as a versatile building block in the synthesis of complex peptide structures, facilitating advancements in therapeutic applications.

Cyclohexanepentanoic acid, γ-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-β-hydroxy-, [S-(R*,R*)]- (9CI)

(3S,4S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-cyclohexyl-3-hydroxypentanoic acid

CAS 130597-31-8

Fmoc-ACHPA

Cyclohexanepentanoic acid, γ-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-β-hydroxy-, [S-(R,R)]- (9CI)

Ref: IN-DA000UOC

(3S,4S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-cyclohexyl-3-hydroxypentanoic acid

Ref: 54-OR1067981