CAS 151910-11-1

(1S,2R)-N-BOC-1-Amino-2-phenylcyclopropanecarboxylic acid

Description:

(1S,2R)-N-BOC-1-Amino-2-phenylcyclopropanecarboxylic acid is a chiral compound characterized by its cyclopropane structure, which features a phenyl group and a carboxylic acid functional group. The "N-BOC" designation indicates the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino group, which is commonly used in peptide synthesis to protect amines. The specific stereochemistry, denoted by (1S,2R), refers to the spatial arrangement of atoms around the chiral centers, influencing the compound's reactivity and interactions in biological systems. This compound is of interest in medicinal chemistry and drug development due to its potential applications in synthesizing biologically active molecules. Its unique structure may contribute to specific binding interactions with biological targets, making it a valuable compound for further research in pharmacology and organic synthesis. As with many chiral compounds, the enantiomeric purity and stereochemical configuration are crucial for its efficacy and safety in potential therapeutic applications.

Formula: C₁₅H₁₉NO₄

InChI: InChI=1/C15H19NO4/c1-14(2,3)20-13(19)16-15(12(17)18)9-11(15)10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,16,19)(H,17,18)/t11-,15+/m1/s1

Synonyms:

• (1S,2R)-1-[(tert-butoxycarbonyl)amino]-2-phenylcyclopropanecarboxylate
• (1S,2R)-1-[(tert-butoxycarbonyl)amino]-2-phenylcyclopropanecarboxylic acid

(1S,2R)-1-[(tert-Butoxycarbonyl)amino]-2-phenylcyclopropanecarboxylic acid

CAS: 151910-11-1

(1S,2R)-1-[(tert-Butoxycarbonyl)amino]-2-phenylcyclopropanecarboxylic acid

Purity: 95%

Molecular weight: 277.32g/mol

Ref: 54-OR54839