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CAS 220497-60-9

:

(2S)-4-Bromo-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-pentenoic acid

Description:
(2S)-4-Bromo-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-pentenoic acid is a chemical compound characterized by its unique structure, which includes a bromine atom, a pentenoic acid backbone, and a fluorenylmethoxycarbonyl (Fmoc) protecting group. The presence of the bromine atom introduces notable reactivity, making it useful in various synthetic applications, particularly in peptide synthesis. The Fmoc group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis of peptides and other complex molecules. This compound is typically utilized in organic synthesis and medicinal chemistry, where its ability to facilitate the formation of peptide bonds is valuable. Additionally, the stereochemistry indicated by the (2S) designation suggests that the compound has specific spatial arrangements that can influence its biological activity and interactions. Overall, this compound exemplifies the intricate design often found in synthetic organic chemistry, combining functional groups that enable diverse chemical transformations.
Formula:C20H18BrNO4
InChI:InChI=1S/C20H18BrNO4/c1-12(21)10-18(19(23)24)22-20(25)26-11-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,1,10-11H2,(H,22,25)(H,23,24)/t18-/m0/s1
InChI key:InChIKey=BYQROHMHEGJMPD-SFHVURJKSA-N
SMILES:C(OC(N[C@@H](CC(Br)=C)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (2S)-4-Bromo-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-pentenoic acid
  • (2S)-4-bromo-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-enoate
  • (2S)-4-bromo-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-enoic acid
  • (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromopent-4-enoic acid
  • (S)-N-(9-Fluorenylmethoxycarbonyl)-2-amino-4-bromo-4-pentenoic acid
  • 4-Pentenoic acid, 4-bromo-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2S)-
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