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CAS 190897-47-3

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(S)-3-(BOC-AMINO)-2-METHYLPROPIONIC ACID

Description:
(S)-3-(BOC-AMINO)-2-METHYLPROPIONIC ACID, with the CAS number 190897-47-3, is a chiral amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino functional group. This compound features a branched aliphatic structure, which includes a methyl group and a propionic acid moiety, contributing to its unique properties. The BOC group is commonly used in organic synthesis to protect amines during chemical reactions, allowing for selective functionalization of other reactive sites. As a chiral compound, it exists in two enantiomeric forms, with the (S)-configuration being biologically relevant in various applications, particularly in pharmaceuticals and peptide synthesis. The presence of the carboxylic acid group imparts acidic characteristics, making it soluble in polar solvents. This compound is often utilized in the synthesis of peptides and other bioactive molecules, highlighting its importance in medicinal chemistry and drug development. Its stability and reactivity can be influenced by the surrounding conditions, including pH and temperature, making it a versatile building block in organic synthesis.
Formula:C9H17NO4
InChI:InChI=1/C9H17NO4/c1-6(7(11)12)5-10-8(13)14-9(2,3)4/h6H,5H2,1-4H3,(H,10,13)(H,11,12)/t6-/m0/s1
SMILES:C[C@@H](CN=C(O)OC(C)(C)C)C(=O)O
Synonyms:
  • Boc-S-3-Aminoisobutyric acid
  • Propanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-methyl-, (2S)- (9CI)
  • (S)-Boc-Β2-Homoala-Oh
  • 2S-Methyl-3-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-Propanoic Acid
  • (2S)-3-[(tert-butoxycarbonyl)amino]-2-methylpropanoic acid
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