CAS 161330-30-9
:2-FLUOROPHENYLGLYCINE-N-BOC PROTECTED
Description:
2-Fluorophenylglycine-N-BOC protected, with the CAS number 161330-30-9, is an organic compound that features a fluorinated aromatic ring and an amino acid structure. The "N-BOC protected" designation indicates that the amine group is protected by a tert-butyloxycarbonyl (BOC) group, which is commonly used in peptide synthesis to prevent unwanted reactions during the formation of peptide bonds. This compound typically exhibits characteristics such as moderate solubility in organic solvents and potential reactivity due to the presence of both the amino and carboxylic acid functional groups. The fluorine atom on the phenyl ring can influence the compound's electronic properties, potentially affecting its reactivity and interactions in biological systems. As a derivative of phenylglycine, it may be of interest in medicinal chemistry and drug development, particularly in the synthesis of biologically active compounds. Proper handling and storage are essential, as with many organic chemicals, to ensure safety and stability.
Formula:C13H16FNO4
InChI:InChI=1/C13H16FNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-6-4-5-7-9(8)14/h4-7,10H,1-3H3,(H,15,18)(H,16,17)
SMILES:CC(C)(C)OC(=NC(c1ccccc1F)C(=O)O)O
Synonyms:- N-Boc-2-Fluorophenylglycine
- [(Tert-Butoxycarbonyl)Amino](2-Fluorophenyl)Acetic Acid
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Found 3 products.
N-BOC-(2-Fluorophenyl)glycine
CAS:Formula:C13H16FNO4Purity:97%Color and Shape:SolidMolecular weight:269.26882-Fluoro-DL-phenylglycine, N-BOC protected
CAS:<p>2-Fluoro-DL-phenylglycine, N-BOC protected</p>Formula:C13H16FNO4Purity:95%Color and Shape: white solidMolecular weight:269.27g/mol2-((tert-Butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid
CAS:Purity:97%Molecular weight:269.2720032


