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CAS 1018332-24-5

:

1-(1,1-Dimethylethyl) (2R,4R)-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1,2-pyrrolidinedicarboxylate

Description:
1-(1,1-Dimethylethyl) (2R,4R)-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1,2-pyrrolidinedicarboxylate is a complex organic compound characterized by its unique structural features, including a pyrrolidine ring 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 chemical reactions. The presence of the dimethyl group enhances its steric properties, influencing its reactivity and solubility. The compound is likely to be a solid at room temperature, with moderate solubility in organic solvents. Its molecular structure suggests potential for specific interactions in biological systems, making it of interest in medicinal chemistry. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its practical applications. Overall, this compound exemplifies the complexity and utility of modern organic molecules in synthetic chemistry.
Formula:C25H28N2O6
InChI:InChI=1S/C25H28N2O6/c1-25(2,3)33-24(31)27-13-15(12-21(27)22(28)29)26-23(30)32-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20-21H,12-14H2,1-3H3,(H,26,30)(H,28,29)/t15-,21-/m1/s1
InChI key:InChIKey=UPXRTVAIJMUAQR-QVKFZJNVSA-N
SMILES:C(OC(N[C@H]1CN(C(OC(C)(C)C)=O)[C@@H](C(O)=O)C1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • 1-(1,1-Dimethylethyl) (2R,4R)-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1,2-pyrrolidinedicarboxylate
  • 1,2-Pyrrolidinedicarboxylic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, 1-(1,1-dimethylethyl) ester, (2R,4R)-
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