CAS 218608-97-0
:Boc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid
Description:
Boc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group, an amino group, and a fluoro-substituted phenyl moiety. This compound is typically used in peptide synthesis and medicinal chemistry due to its ability to serve as a building block for more complex molecules. The presence of the Boc group provides stability and protection to the amino group during synthetic procedures, allowing for selective reactions. The (S) configuration indicates that it is a chiral molecule, which is significant in biological systems where stereochemistry can influence activity and interactions. The 4-fluorophenyl group enhances the compound's lipophilicity and may influence its pharmacological properties. Overall, Boc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid is notable for its utility in drug development and its role in the synthesis of biologically active compounds.
Formula:C15H20FNO4
InChI:InChI=1/C15H20FNO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-4-6-11(16)7-5-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc(cc1)F)CC(=O)O)O
Synonyms:- (3S)-3-[(tert-butoxycarbonyl)amino]-4-(4-fluorophenyl)butanoic acid
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Found 3 products.
Boc-(s)-3-amino-4-(4-fluoro-phenyl)-butyric acid
CAS:Formula:C15H20FNO4Purity:98%Color and Shape:SolidMolecular weight:297.3220(S)-3-((tert-Butoxycarbonyl)amino)-4-(4-fluorophenyl)butanoic acid
CAS:<p>(S)-3-((tert-Butoxycarbonyl)amino)-4-(4-fluorophenyl)butanoic acid</p>Purity:97%Molecular weight:297.33g/mol(S)-3-((tert-Butoxycarbonyl)amino)-4-(4-fluorophenyl)butanoic acid
CAS:Formula:C15H20FNO4Purity:97%Molecular weight:297.326



