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CAS 270596-37-7

:

(βS)-2-Chloro-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid

Description:
(βS)-2-Chloro-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid, with CAS number 270596-37-7, is a synthetic organic compound characterized by its complex structure, which includes a chloro group, a fluorenylmethoxycarbonyl (Fmoc) protecting group, and a benzenebutanoic acid moiety. This compound is typically used in peptide synthesis and other organic chemistry applications due to its ability to protect amino groups during reactions. The presence of the Fmoc group allows for selective deprotection under mild basic conditions, facilitating the synthesis of peptides. The chloro substituent may also play a role in enhancing reactivity or solubility in various solvents. Overall, this compound is notable for its utility in the field of medicinal chemistry and peptide research, where precise modifications of amino acids are crucial for developing bioactive molecules. Its specific stereochemistry, indicated by the (βS) designation, suggests a particular spatial arrangement that can influence its biological activity and interactions.
Formula:C25H22ClNO4
InChI:InChI=1S/C25H22ClNO4/c26-23-12-6-1-7-16(23)13-17(14-24(28)29)27-25(30)31-15-22-20-10-4-2-8-18(20)19-9-3-5-11-21(19)22/h1-12,17,22H,13-15H2,(H,27,30)(H,28,29)/t17-/m0/s1
InChI key:InChIKey=RTGMPAHEDKUNFP-KRWDZBQOSA-N
SMILES:C(OC(N[C@@H](CC1=C(Cl)C=CC=C1)CC(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (3S)-4-(2-chlorophenyl)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}butanoic acid
  • (βS)-2-Chloro-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]benzenebutanoic acid
  • Benzenebutanoic acid, 2-chloro-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βS)-
  • Fmoc-β-HoPhe(2-Cl)-OH
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