CAS 159990-12-2
:(S)-Boc-4-methoxy-β-Phe-OH
Description:
(S)-Boc-4-methoxy-β-Phe-OH, with the CAS number 159990-12-2, is a chemical compound that belongs to the class of amino acids and derivatives. It features a protected amino group, indicated by the Boc (tert-butyloxycarbonyl) group, which is commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. The compound contains a β-phenylalanine structure, characterized by the presence of a phenyl group attached to the β-carbon of the amino acid backbone. The methoxy group at the 4-position of the phenyl ring enhances the compound's lipophilicity and may influence its biological activity. This compound is typically utilized in the synthesis of peptides and other bioactive molecules, making it valuable in pharmaceutical research and development. Its stereochemistry, denoted by the (S) configuration, indicates that it is the S-enantiomer, which can have distinct properties and biological activities compared to its R counterpart. Overall, (S)-Boc-4-methoxy-β-Phe-OH is an important intermediate in organic synthesis and medicinal chemistry.
Formula:C15H21NO5
InChI:InChI=1/C15H21NO5/c1-15(2,3)21-14(19)16-12(9-13(17)18)10-5-7-11(20-4)8-6-10/h5-8,12H,9H2,1-4H3,(H,16,19)(H,17,18)/t12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CC(=O)O)c1ccc(cc1)OC)O
Synonyms:- (3S)-3-[(tert-butoxycarbonyl)amino]-3-(4-methoxyphenyl)propanoic acid
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Found 4 products.
Boc-(s)-3-amino-3-(4-methoxy-phenyl)-propionic acid
CAS:Formula:C15H21NO5Purity:95%Color and Shape:SolidMolecular weight:295.3309(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid
CAS:(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acidPurity:95%Molecular weight:295.33g/mol(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-methoxyphenyl)propanoic acid
CAS:Formula:C15H21NO5Purity:98%Color and Shape:SolidMolecular weight:295.335




