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CAS 101759-74-4

:

(2S)-2-[[(1,1-Dimethylethoxy)carbonyl]methylamino]butanoic acid

Description:
(2S)-2-[[(1,1-Dimethylethoxy)carbonyl]methylamino]butanoic acid, with CAS number 101759-74-4, is an amino acid derivative characterized by its specific stereochemistry and functional groups. This compound features a butanoic acid backbone, which is a four-carbon chain terminating in a carboxylic acid group, and it contains an amino group that is substituted with a dimethylethoxycarbonyl group. The presence of the dimethylethoxycarbonyl moiety contributes to its stability and solubility in organic solvents. The stereochemistry at the second carbon (2S) indicates that it has a specific three-dimensional arrangement, which is crucial for its biological activity and interactions. This compound may be utilized in various applications, including pharmaceutical synthesis and as a building block in peptide chemistry. Its unique structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry and drug development. As with many amino acid derivatives, it may exhibit properties such as chirality, solubility in polar solvents, and reactivity with other functional groups.
Formula:C10H19NO4
InChI:InChI=1S/C10H19NO4/c1-6-7(8(12)13)11(5)9(14)15-10(2,3)4/h7H,6H2,1-5H3,(H,12,13)/t7-/m0/s1
InChI key:InChIKey=QIXDRLIEARGEQY-ZETCQYMHSA-N
SMILES:[C@@H](N(C(OC(C)(C)C)=O)C)(C(O)=O)CC
Synonyms:
  • (2S)-2-[[(1,1-Dimethylethoxy)carbonyl]methylamino]butanoic acid
  • (S)-2-(N-Methyl-N-(tert-butoxycarbonyl)amino)butanoic acid
  • (S)-2-[(tert-Butoxycarbonyl)(methyl)amino]butyric acid
  • (S)-2-[tert-Butoxycarbonyl(methyl)amino]butanoic acid
  • Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-, (2S)-
  • N-Boc-(S)-2-(methylamino)butyric acid
  • Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-, (S)-
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