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CAS 114360-55-3

:

(2R)-2-Amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]butanoic acid

Description:
(2R)-2-Amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]butanoic acid, commonly known as a derivative of amino acids, exhibits several notable characteristics. This compound features a chiral center, which contributes to its specific stereochemistry, denoted by the (2R) configuration. It contains an amino group (-NH2), a carboxylic acid group (-COOH), and a side chain that includes a dimethylethoxycarbonyl group, which enhances its stability and solubility in organic solvents. The presence of these functional groups suggests that it can participate in various chemical reactions, including peptide bond formation, making it relevant in biochemical applications. Additionally, its structure indicates potential for use in pharmaceutical formulations due to its ability to interact with biological systems. The compound is typically synthesized through specific organic reactions, and its purity and stability are crucial for its application in research and industry. Overall, this amino acid derivative is significant in the fields of medicinal chemistry and biochemistry, particularly in the development of peptide-based therapeutics.
Formula:C9H18N2O4
InChI:InChI=1S/C9H18N2O4/c1-9(2,3)15-8(14)11-5-4-6(10)7(12)13/h6H,4-5,10H2,1-3H3,(H,11,14)(H,12,13)/t6-/m1/s1
InChI key:InChIKey=ICJFZQLAIOCZNG-ZCFIWIBFSA-N
SMILES:C(OC(C)(C)C)(NCC[C@H](C(O)=O)N)=O
Synonyms:
  • (2R)-2-Amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
  • (2R)-2-Amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]butanoic acid
  • (2R)-2-Amino-4-[[(tert-butoxy)carbonyl]amino]butanoic acid
  • (R)-2-Amino-4-((tert-butoxycarbonyl)amino)butanoic acid
  • Butanoic acid, 2-amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2R)-
  • Butanoic acid, 2-amino-4-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-
  • N-Gamma-T-Butoxycarbonyl-D-2,4-Diaminobutyric Acid
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