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CAS 145206-40-2

:

(S)-N-BOC-2-Furylalanine

Description:
(S)-N-BOC-2-Furylalanine is a synthetic amino acid derivative characterized by the presence of a furan ring and a tert-butyloxycarbonyl (BOC) protecting group on the amino group. This compound is typically used in peptide synthesis and as a building block in the development of pharmaceuticals due to its unique structural features that can influence biological activity. The furan moiety contributes to its aromatic properties, while the BOC group provides stability and protection during chemical reactions. The (S) configuration indicates that it is the S-enantiomer, which is often biologically relevant, as many amino acids exist in this form in nature. The compound is generally soluble in organic solvents and may exhibit specific reactivity patterns typical of amino acids, such as participating in peptide bond formation. Its molecular structure allows for potential interactions in biological systems, making it a valuable compound in medicinal chemistry and drug design.
Formula:C24H40N2O5
InChI:InChI=1/C12H17NO5.C12H23N/c1-12(2,3)18-11(16)13-9(10(14)15)7-8-5-4-6-17-8;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15);11-13H,1-10H2/t9-;/m1./s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1ccco1)C(=O)O)O.C1CCC(CC1)NC1CCCCC1
Synonyms:
  • N-tert-Butoxycarbonyl-2-furyl-L-alanine
  • Boc-L-2-Furylalanine-DCHA
  • Boc-L-3-(2-Furyl)-Alanine・Dcha
  • N-(tert-butoxycarbonyl)-3-furan-2-yl-L-alanine
  • (2S)-2-[(tert-butoxycarbonyl)amino]-3-furan-2-ylpropanoate
  • N-(tert-butoxycarbonyl)-3-furan-2-yl-L-alanine - N-cyclohexylcyclohexanamine (1:1)
  • N-(tert-butoxycarbonyl)-3-furan-2-yl-D-alanine - N-cyclohexylcyclohexanamine (1:1)
  • Boc-L-2-Furylalanine・DCHA
  • Boc-3-(2-Furyl)-L-alanine
  • Boc-L-2-Furylalanine Dcha Salt
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