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CAS 84311-19-3

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N-[(1,1-Dimethylethoxy)carbonyl]-2-methyl-L-serine

Description:
N-[(1,1-Dimethylethoxy)carbonyl]-2-methyl-L-serine, with the CAS number 84311-19-3, is an amino acid derivative characterized by the presence of a carbonyl group and a dimethylethoxy protective group. This compound features a chiral center, which contributes to its potential biological activity and specificity in various applications, particularly in peptide synthesis and medicinal chemistry. The dimethylethoxy group serves as a protecting group, enhancing the stability of the molecule during chemical reactions. The presence of the methyl group on the serine backbone may influence its solubility and reactivity. This compound is typically used in research settings, particularly in the synthesis of peptides and other bioactive molecules, due to its ability to participate in various chemical transformations. Its structural characteristics suggest potential interactions with biological systems, making it of interest in pharmacological studies. As with many amino acid derivatives, careful handling and storage are recommended to maintain its integrity and reactivity.
Formula:C9H17NO5
InChI:InChI=1S/C9H17NO5/c1-8(2,3)15-7(14)10-9(4,5-11)6(12)13/h11H,5H2,1-4H3,(H,10,14)(H,12,13)/t9-/m0/s1
InChI key:InChIKey=FWRXDSRYWWYTPD-VIFPVBQESA-N
SMILES:N([C@](C(O)=O)(CO)C)C(OC(C)(C)C)=O
Synonyms:
  • (2S)-2-[[(tert-Butoxy)carbonyl]amino]-3-hydroxy-2-methylpropanoic acid
  • (S)-2-(tert-Butoxycarbonylamino)-3-hydroxy-2-methylpropanoic acid
  • <span class="text-smallcaps">L</span>-Serine, N-[(1,1-dimethylethoxy)carbonyl]-2-methyl-
  • L-serine, N-[(1,1-dimethylethoxy)carbonyl]-2-methyl-
  • N-Boc-α-methyl-L-serine
  • N-[(1,1-Dimethylethoxy)carbonyl]-2-methyl-<span class="text-smallcaps">L</span>-serine
  • N-[(1,1-Dimethylethoxy)carbonyl]-2-methyl-L-serine
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