The chemical substance known as (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,3-dimethoxybenzenepropanoic acid, with the CAS number 511272-39-2, is a synthetic compound that features a complex structure characterized by the presence of a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis. This compound contains a propanoic acid moiety, indicating it has acidic properties, and is further substituted with methoxy groups on the aromatic ring, which can influence its solubility and reactivity. The stereochemistry indicated by (βR) suggests that the compound has a specific three-dimensional arrangement, which can be crucial for its biological activity. The presence of the Fmoc group also suggests potential applications in organic synthesis, particularly in the field of medicinal chemistry and peptide development. Overall, this compound's unique structural features may contribute to its utility in various chemical and pharmaceutical applications.

(βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,3-dimethoxybenzenepropanoic acid

511272-39-2: (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,3-dimethoxybenzenepropanoic acid, Benzenepropanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2,3-dimethoxy-, (βR)-

CAS 511272-39-2: (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2,3-dimethoxybenzenepropanoic acid

Fmoc-(R)-3-Amino-3-(2,3-dimethoxy-phenyl)-propionic acid

Ref: 10-F765137

Fmoc-(R)-3-amino-3-(2,3-dimethoxy-phenyl)-propionic acid

Ref: 3D-LVA27239

FMOC-(R)-3-AMINO-3-(2,3-DIMETHOXY-PHENYL)-PROPIONIC ACID

Ref: IN-DA00D89U