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TERT.-BUTYLAMMONIUM_SALT_OF_3,4-DICHLOROPHENOXYMETHYL_2',5'-DI-O-TETRAHYDROPYRAN-2-YL-3'-O-URIDINE_PHOSPHATE
SpectraBase Compound ID 3GcqAzuAi0n
InChI InChI=1S/C26H33Cl2N2O12P.C4H11N/c27-17-8-7-16(13-18(17)28)38-15-39-43(33,34)42-23-19(14-37-21-5-1-3-11-35-21)40-25(30-10-9-20(31)29-26(30)32)24(23)41-22-6-2-4-12-36-22;1-4(2,3)5/h7-10,13,19,21-25H,1-6,11-12,14-15H2,(H,33,34)(H,29,31,32);5H2,1-3H3/t19-,21?,22?,23-,24-,25-;/m0./s1
InChIKey IDGAFQFHVFQDHS-SHZKZJQPSA-N
Mol Weight 740.6 g/mol
Molecular Formula C30H44Cl2N3O12P
Exact Mass 739.203966 g/mol
Enantiomer InChIKey IDGAFQFHVFQDHS-NXNYEHAGSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
General base catalysis vs. medium effects in the hydrolysis of an RNA modelElectronic supplementary information (ESI) available: tables of primary kinetic data and derived rate constants. See http://www.rsc.org/suppdata/p2/b1/b109325h/ Journal of the Chemical Society, Perkin Transactions 2 2002

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