CymitQuimica logo

CAS 332064-94-5

:

(3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hex-5-ynoic acid

Description:
(3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hex-5-ynoic acid is a synthetic organic compound characterized by its unique structure, which includes a hexynoic acid backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group on the amino functional group. This compound is typically used in peptide synthesis as a building block, particularly in the formation of peptides where the Fmoc group serves as a protective moiety for the amino group during coupling reactions. The presence of the alkyne functional group (hex-5-ynoic acid) allows for potential applications in click chemistry and other coupling reactions. The stereochemistry at the 3-position is crucial for its biological activity and interaction with other molecules. Additionally, the compound is likely to exhibit solubility in organic solvents, while its acidic nature is attributed to the carboxylic acid group, which can participate in various chemical reactions. Overall, this compound is significant in the field of organic synthesis and medicinal chemistry, particularly in the development of peptide-based therapeutics.
Formula:C21H19NO4
InChI:InChI=1/C21H19NO4/c1-2-7-14(12-20(23)24)22-21(25)26-13-19-17-10-5-3-8-15(17)16-9-4-6-11-18(16)19/h1,3-6,8-11,14,19H,7,12-13H2,(H,22,25)(H,23,24)/t14-/m1/s1
SMILES:C#CC[C@H](CC(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • (3R)-3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-hexynoic acid
  • 5-hexynoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (3R)-
  • Fmoc-D-β-HoGly(Propargyl)-OH
  • Fmoc-(R)-3-Amino-5-Hexynoic Acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.