Abstract [2955‐74‐0] C9H10N2O7S (MW 290.28) InChI = 1S/C9H10N2O7S/c1‐2‐17‐9(12)10‐18‐19(15,16)8‐5‐3‐7(4‐6‐8)11(13)14/h3‐6H,2H2,1H3,(H,10,12) InChIKey = XBTJZULRZQBGIT‐UHFFFAOYSA‐N (generation of ethoxycarbonylnitrene by α‐elimination2, 3 under mild conditions, including phase‐transfer conditions4) Physical Data : mp 116.4–116.8 °C. Solubility : sol ether, acetone, CHCl3, CH2Cl2, DMSO, DMF, ethyl acetate, alcohols; moderately sol benzene; insol hydrocarbon solvents, CCl4, H2O. Preparative Method : by the reaction of N ‐hydroxyurethane with p ‐nitrobenzenesulfonyl chloride.2
p-Nitrobenzenesulfonyloxyurethane / Pearson, William H.; Ramamoorthy, P. Sivaramakrishnan; Pellacani, Lucio. - (2019). [10.1002/047084289X.rn025.pub2].
p-Nitrobenzenesulfonyloxyurethane
Pellacani, Lucio
2019
Abstract
Abstract [2955‐74‐0] C9H10N2O7S (MW 290.28) InChI = 1S/C9H10N2O7S/c1‐2‐17‐9(12)10‐18‐19(15,16)8‐5‐3‐7(4‐6‐8)11(13)14/h3‐6H,2H2,1H3,(H,10,12) InChIKey = XBTJZULRZQBGIT‐UHFFFAOYSA‐N (generation of ethoxycarbonylnitrene by α‐elimination2, 3 under mild conditions, including phase‐transfer conditions4) Physical Data : mp 116.4–116.8 °C. Solubility : sol ether, acetone, CHCl3, CH2Cl2, DMSO, DMF, ethyl acetate, alcohols; moderately sol benzene; insol hydrocarbon solvents, CCl4, H2O. Preparative Method : by the reaction of N ‐hydroxyurethane with p ‐nitrobenzenesulfonyl chloride.2| File | Dimensione | Formato | |
|---|---|---|---|
|
Pearson_p-Nitrobenzenesulfonyloxyurethane_2019.pdf
solo gestori archivio
Note: https://onlinelibrary.wiley.com/doi/abs/10.1002/047084289X.rn025.pub2
Tipologia:
Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza:
Tutti i diritti riservati (All rights reserved)
Dimensione
196.55 kB
Formato
Adobe PDF
|
196.55 kB | Adobe PDF | Contatta l'autore |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
