CAS 1310680-35-3

(2R)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3,3-dimethyl-4-pentenoic acid

Description:

The chemical substance known as (2R)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3,3-dimethyl-4-pentenoic acid, with the CAS number 1310680-35-3, is a synthetic compound primarily used in peptide synthesis and as a building block in organic chemistry. This compound features a chiral center, which contributes to its stereochemistry, specifically the (2R) configuration. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates its utility in protecting amino groups during peptide synthesis, allowing for selective reactions. The structure includes a pentenoic acid moiety, which introduces unsaturation and can influence the compound's reactivity and physical properties. The dimethyl substitution at the 3-position enhances steric hindrance, potentially affecting the compound's conformation and interactions. Overall, this compound is characterized by its complex structure, functional groups that facilitate chemical transformations, and its role in the synthesis of more complex biomolecules.

Formula: C₂₂H₂₃NO₄

InChI: InChI=1S/C22H23NO4/c1-4-22(2,3)19(20(24)25)23-21(26)27-13-18-16-11-7-5-9-14(16)15-10-6-8-12-17(15)18/h4-12,18-19H,1,13H2,2-3H3,(H,23,26)(H,24,25)/t19-/m0/s1

InChI key: InChIKey=KSFBTMRFQUMTJS-IBGZPJMESA-N

SMILES: C(OC(N[C@H](C(C=C)(C)C)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2

Synonyms:

• (2R)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3,3-dimethyl-4-pentenoic acid
• (R)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3,3-dimethylpent-4-enoic acid
• 4-Pentenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-3,3-dimethyl-, (2R)-
• (2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3,3-dimethylpent-4-enoic acid
• (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3,3-dimethylpent-4-enoic acid