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CAS 1655-57-8

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N-(2,4-Dinitrophenyl)-L-leucine

Description:
N-(2,4-Dinitrophenyl)-L-leucine, with the CAS number 1655-57-8, is an amino acid derivative characterized by the presence of a dinitrophenyl group attached to the amino acid leucine. This compound is typically used in biochemical research, particularly in studies involving protein synthesis and enzyme activity. The dinitrophenyl group serves as a chromophore, allowing for the detection and quantification of the compound through spectrophotometric methods. N-(2,4-Dinitrophenyl)-L-leucine is known for its relatively high solubility in organic solvents and moderate solubility in water, which can influence its reactivity and interactions in biological systems. The compound exhibits properties typical of amino acids, including the ability to participate in peptide bond formation. Additionally, due to the presence of the dinitrophenyl moiety, it can undergo electrophilic substitution reactions, making it a useful reagent in organic synthesis. Safety precautions should be taken when handling this compound, as the dinitrophenyl group can be hazardous.
Formula:C12H15N3O6
InChI:InChI=1S/C12H15N3O6/c1-7(2)5-10(12(16)17)13-9-4-3-8(14(18)19)6-11(9)15(20)21/h3-4,6-7,10,13H,5H2,1-2H3,(H,16,17)/t10-/m0/s1
InChI key:InChIKey=STMDPCBYJCIZOD-JTQLQIEISA-N
SMILES:N([C@@H](CC(C)C)C(O)=O)C1=C(N(=O)=O)C=C(N(=O)=O)C=C1
Synonyms:
  • (2,4-Dinitrophenyl)-<span class="text-smallcaps">L</span>-leucine
  • (2S)-2-[(2,4-Dinitrophenyl)amino]-4-methylpentanoic acid
  • <span class="text-smallcaps">L</span>-DNP-Leucine
  • <span class="text-smallcaps">L</span>-Leucine, N-(2,4-dinitrophenyl)-
  • DNP-<span class="text-smallcaps">L</span>-leucine
  • DNP-L-Leucine 2,4-Dinitrophenyl-L-leucine
  • Leucine, N-(2,4-dinitrophenyl)-, <span class="text-smallcaps">L</span>-
  • N-(2,4-Dinitrophenyl)-<span class="text-smallcaps">L</span>-leucine
  • N-(2,4-Dinitrophenyl)-L-leucine
  • N-2,4-DNP-<span class="text-smallcaps">L</span>-leucine
  • See more synonyms
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