3',5'-DI-O-LEVULINYL-2'-O-(2-METHOXYETHYL)-5-METHYLCYTIDINE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | G5qtUeJFb4h |
|---|---|
| InChI | InChI=1S/C23H33N3O10/c1-13-11-26(23(31)25-21(13)24)22-20(33-10-9-32-4)19(36-18(30)8-6-15(3)28)16(35-22)12-34-17(29)7-5-14(2)27/h11,16,19-20,22H,5-10,12H2,1-4H3,(H2,24,25,31)/t16-,19-,20-,22-/m0/s1 |
| InChIKey | IVQKCLSTYQPKIL-CJFIXGCPSA-N |
| Mol Weight | 511.5 g/mol |
| Molecular Formula | C23H33N3O10 |
| Exact Mass | 511.216594 g/mol |
| Enantiomer InChIKey | IVQKCLSTYQPKIL-KREFBHGWSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
3',5'-DI-O-LEVULINYL-2'-O-METHOXYETHYL-5-METHYLURIDINE
N-BENZOYL-5'-O-LEVULINYL-2'-O-(2-METHOXYETHYL)-5-METHYLCYTIDINE
Cytidine, N-acetyl-N-methyl-, 2',3',5'-triacetate
BWPKOVBKNIGFLC-WNHJNPCNSA-N
GMVOGFKODHTPBT-LEAZDLGRSA-N
SUMQAHHZUFTWSL-QZHFEQFPSA-N
Trimethylsilyl derivative of 3,n4-ethanocytidine
MXTGSNUNMUJJOU-KNTRFNDTSA-N
HKCJQMUIZXVQRF-QZHFEQFPSA-N
CCJAHNUJEPWDFO-WNHJNPCNSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Building Blocks for the Solution Phase Synthesis of Oligonucleotides: Regioselective Hydrolysis of 3‘,5‘-Di-O-levulinylnucleosides Using an Enzymatic Approach | The Journal of Organic Chemistry | 2002 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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