CAS 1108622-91-8

3-Quinolinepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)-

Description:

3-Quinolinepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)- is a chemical compound characterized by its complex structure, which includes a quinoline moiety and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is typically used in peptide synthesis and other organic synthesis applications due to its ability to protect amino groups during reactions. The presence of the quinoline ring contributes to its aromatic properties, which can influence its reactivity and solubility. The Fmoc group is commonly employed in solid-phase peptide synthesis, allowing for selective deprotection under mild conditions. The (αR) designation indicates the specific stereochemistry at the alpha carbon, which can be crucial for biological activity and interaction with biological targets. Overall, this compound is significant in medicinal chemistry and biochemistry, particularly in the development of pharmaceuticals and biologically active molecules. Its unique structural features make it a valuable tool in synthetic organic chemistry.

Formula: C₂₇H₂₂N₂O₄

Synonyms:

• (2R)-2-[(FLUOREN-9-YLMETHOXY)CARBONYLAMINO]-3-(3-QUINOLYL)PROPANOIC ACID
• (2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(quinolin-3-yl)propanoic acid
• 3-Quinolinepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)-
• Fmoc-3-(3-Quinolyl)-D-Ala-OH
• (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(quinolin-3-yl)propanoic acid

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(quinolin-3-yl)propanoic acid

CAS: 1108622-91-8

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(quinolin-3-yl)propanoic acid

Purity: 95%

Molecular weight: 438.48g/mol

Ref: 54-OR1052949