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CAS 170642-29-2

:

Cyclopropanepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (R)-

Description:
Cyclopropanepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (R)-, with CAS number 170642-29-2, is a chemical compound characterized by its unique structural features, including a cyclopropane ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is typically used in peptide synthesis, particularly in the protection of amino groups during the formation of peptide bonds. The presence of the Fmoc group allows for selective deprotection under mild basic conditions, facilitating the stepwise assembly of peptides. The (R)- configuration indicates that it is a chiral molecule, which can exhibit specific optical activity. Its properties include solubility in organic solvents, and it may have applications in medicinal chemistry and drug development due to its structural complexity. The compound's reactivity is influenced by the functional groups present, making it a valuable intermediate in organic synthesis. Overall, its characteristics make it an important compound in the field of organic and medicinal chemistry.
Formula:C21H21NO4
InChI:InChI=1S/C21H21NO4/c23-20(24)19(11-13-9-10-13)22-21(25)26-12-18-16-7-3-1-5-14(16)15-6-2-4-8-17(15)18/h1-8,13,18-19H,9-12H2,(H,22,25)(H,23,24)/t19-/m1/s1
InChI key:InChIKey=DRGUEWQZLABTFG-LJQANCHMSA-N
SMILES:C(OC(N[C@H](CC1CC1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (2R)-3-Cyclopropyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid
  • 3-cyclopropyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanine
  • 3-cyclopropyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine
  • Cyclopropanepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (R)-
  • Fmoc-(R)-3-Cyclopropylalanine
  • Fmoc-<span class="text-smallcaps">D</span>-Cpa-OH
  • Fmoc-D-Cyclopropylalanine
  • Fmoc-D-Cpa-OH
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