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CAS 219819-76-8

:

(2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hexenoic acid

Description:
(2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hexenoic acid, with CAS number 219819-76-8, is an organic compound characterized by its unique structure that includes a hexenoic acid backbone and a dimethylethoxycarbonyl group. This compound features a chiral center at the second carbon, which contributes to its stereochemistry and potential biological activity. The presence of the amino group indicates that it can participate in various chemical reactions, including peptide bond formation. The hexenoic acid portion suggests that it may exhibit unsaturation, which can influence its reactivity and interactions with other molecules. This compound may be of interest in pharmaceutical chemistry, particularly in the design of amino acid derivatives or as a building block for more complex molecules. Its specific properties, such as solubility, melting point, and reactivity, would depend on the surrounding conditions and the presence of other functional groups. Overall, this compound exemplifies the complexity and versatility of organic molecules in chemical synthesis and biological applications.
Formula:C11H19NO4
InChI:InChI=1S/C11H19NO4/c1-5-6-7-8(9(13)14)12-10(15)16-11(2,3)4/h5,8H,1,6-7H2,2-4H3,(H,12,15)(H,13,14)/t8-/m1/s1
InChI key:InChIKey=LQIMZUPFMSNHTM-MRVPVSSYSA-N
SMILES:[C@@H](NC(OC(C)(C)C)=O)(CCC=C)C(O)=O
Synonyms:
  • (2r)-2-(Boc-amino)-5-hexenoic acid
  • 5-Hexenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2R)-
  • (2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hexenoic acid
  • Boc-R4-NM
  • (Tert-Butoxy)Carbonyl D-Homoallylglycine
  • (R)-2-((tert-Butoxycarbonyl)amino)hex-5-enoic acid
  • (R)-N-Boc-2-(3'-butenyl)glycine
  • (2R)-2-[(TERT-BUTOXYCARBONYL)AMINO]-5-HEXENOIC ACID
  • (2R)-2-{[(tert-butoxy)carbonyl]amino}hex-5-enoic acid
  • (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hex-5-enoic acid
  • Boc-(R)?-?2-?Amino-?5-?hexenoic acid
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