The chemical substance known as (2S,3R,4E)-2-azido-4-octadecene-1,3-diol, with the CAS number 103348-49-8, is an organic compound characterized by its azido functional group and a long hydrocarbon chain. This compound features a stereocenter at the second and third carbon atoms, indicating specific spatial arrangements that can influence its reactivity and interactions. The presence of the double bond in the octadecene chain contributes to its unsaturation, which can affect its physical properties, such as melting and boiling points, as well as its reactivity in chemical reactions, particularly in addition reactions. The hydroxyl groups at the first and third positions provide sites for potential hydrogen bonding, enhancing its solubility in polar solvents and influencing its biological activity. Overall, this compound's unique structure makes it of interest in various fields, including organic synthesis and medicinal chemistry, where azido groups can be utilized for further functionalization or as bioorthogonal handles in chemical biology.

(2S,3R,4E)-2-azido-4-octadecene-1,*3-diol

103348-49-8: The chemical substance known as (2S,3R,4E)-2-azido-4-octadecene-1,3-diol, with the CAS number 103348-49-8, is an organic compound characterized by its azido functional group and a long hydrocarbon chain. This compound features a stereocenter at the second and third carbon atoms, indicating specific spatial arrangements that can influence its reactivity and interactions. The presence of the double bond in the octadecene chain contributes to its unsaturation, which can affect its physical properties, such as melting and boiling points, as well as its reactivity in chemical reactions, particularly in addition reactions. The hydroxyl groups at the first and third positions provide sites for potential hydrogen bonding, enhancing its solubility in polar solvents and influencing its biological activity. Overall, this compound's unique structure makes it of interest in various fields, including organic synthesis and medicinal chemistry, where azido groups can be utilized for further functionalization or as bioorthogonal handles in chemical biology.

<p>Applications A derivative of Sphingosine, a selective inhibitor of protein kinase C activity and phorbol dibutyrate binding in vitro in human platelets; does not inhibit protein kinase A or myosin light chain kinase; inhibits calmodulin-dependent enzymes; natural isomer of sphingosine.<br></p>

CAS 103348-49-8

(2S,3R,4E)-2-azido-4-octadecene-1,*3-diol

Azido-erythro-sphingosine

Ref: TR-A926500