CAS 35891-72-6
:(2S,3E)-2-amino-4-methoxybut-3-enoic acid
Description:
(2S,3E)-2-amino-4-methoxybut-3-enoic acid, also known as a derivative of amino acids, possesses several notable characteristics. This compound features a chiral center at the second carbon, which contributes to its stereochemistry, specifically the (2S) configuration. The presence of a methoxy group (-OCH3) at the fourth carbon enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. The (3E) configuration indicates that the double bond between the third and fourth carbons is in the trans configuration, which can affect the compound's geometric properties and biological activity. As an amino acid derivative, it may participate in various biochemical pathways, potentially acting as a precursor for other biologically relevant molecules. Its CAS number, 35891-72-6, allows for precise identification in chemical databases. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals, biochemistry, and related fields, warranting further investigation into its properties and functions.
Formula:C5H9NO3
InChI:InChI=1/C5H9NO3/c1-9-3-2-4(6)5(7)8/h2-4H,6H2,1H3,(H,7,8)/b3-2+/t4-/m0/s1
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L-2-Amino-4-methoxy-trans-but-3-enoic Acid
CAS:Controlled ProductFormula:C5H9NO3Color and Shape:NeatMolecular weight:131.13
