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CAS 1231709-26-4

:

4-(1,1-Dimethylethyl) hydrogen N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-<span class="text-smallcaps">D</span>-aspartate

Description:
4-(1,1-Dimethylethyl) hydrogen N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-D-aspartate, with CAS number 1231709-26-4, is a chemical compound that belongs to the class of amino acid derivatives. It features a protected aspartate structure, which is commonly used in peptide synthesis and drug development. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that it is likely utilized as a protecting group for the amino functionality during synthetic procedures. The tert-butyl group contributes to the compound's hydrophobic characteristics, influencing its solubility and stability in various solvents. This compound is typically used in research settings, particularly in the synthesis of peptides and other bioactive molecules. Its structural complexity allows for specific interactions in biological systems, making it a valuable tool in medicinal chemistry and biochemistry. As with many synthetic compounds, safety data and handling precautions should be observed, as the biological activity and toxicity profiles may vary based on the context of use.
Formula:C24H27NO6
InChI:InChI=1S/C24H27NO6/c1-23(2,3)31-20(26)13-24(4,21(27)28)25-22(29)30-14-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,19H,13-14H2,1-4H3,(H,25,29)(H,27,28)/t24-/m1/s1
InChI key:InChIKey=STBMKQNEFSJOCS-XMMPIXPASA-N
SMILES:C(OC(N[C@](CC(OC(C)(C)C)=O)(C(O)=O)C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • 4-(1,1-Dimethylethyl) hydrogen N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-D-aspartate
  • D-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methyl-, 4-(1,1-dimethylethyl) ester
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