N4-BENZOYL-1-[(2R,3R,4R,5R)-4-BENZOYLOXYMETHYL-5-(2-HYDROXYETHYL)-3-[(META-TRIFLUOROMETHYL)-BENZOYLOXY]-TETRAHYDROFURAN-2-YL]-CYTOSINE
Compound with spectra: 1 NMR
![N4-BENZOYL-1-[(2R,3R,4R,5R)-4-BENZOYLOXYMETHYL-5-(2-HYDROXYETHYL)-3-[(META-TRIFLUOROMETHYL)-BENZOYLOXY]-TETRAHYDROFURAN-2-YL]-CYTOSINE](/api/compound/D2Uqtjzjjv1.png?ph=true&h=300&w=458 "N4-BENZOYL-1-[(2R,3R,4R,5R)-4-BENZOYLOXYMETHYL-5-(2-HYDROXYETHYL)-3-[(META-TRIFLUOROMETHYL)-BENZOYLOXY]-TETRAHYDROFURAN-2-YL]-CYTOSINE")
| SpectraBase Compound ID | D2Uqtjzjjv1 |
|---|---|
| InChI | InChI=1S/C33H28F3N3O8/c34-33(35,36)23-13-7-12-22(18-23)31(43)47-27-24(19-45-30(42)21-10-5-2-6-11-21)25(15-17-40)46-29(27)39-16-14-26(38-32(39)44)37-28(41)20-8-3-1-4-9-20/h1-14,16,18,24-25,27,29,40H,15,17,19H2,(H,37,38,41,44)/t24-,25-,27-,29-/m0/s1 |
| InChIKey | BSDJQCTWMCUWFU-JVGXHWGJSA-N |
| Mol Weight | 651.6 g/mol |
| Molecular Formula | C33H28F3N3O8 |
| Exact Mass | 651.182849 g/mol |
| Enantiomer InChIKey | BSDJQCTWMCUWFU-GCMXZSHTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N(4)-1-(2'-BENZOYL-3'-BENZOYLOXYMETHYL-6'-TERT.-BUTYLDIPHENYLSILYL-3',5'-DIDEOXY-BETA-ALLO-FURANOSYL)-CYTOSINE
N4-BENZOYL-1-[(2R,3R,4R,5R)-3-ACETOXY-4-ACETOXYMETHYL-5-(2-TERT.-BUTYLDIPHENYLSILYLOXYETHYL)-TETRAHYDROFURAN-2-YL]-CYTOSINE
1-(2'-BENZOYL-3'-BENZOYLOXYMETHYL-6'-TERT.-BUTYLDIPHENYLSILYL-3',5'-DIDEOXY-BETA-ALLO-FURANOSYL)-URACIL
Benzamide, N-[1-[2,3-di-O-acetyl-5-O-[bis(4-methoxyphenyl)phenylmethyl]-.beta.-D-arabinofuranosyl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-4-methoxy-
4-N-TRIFLUOROACETYL-2',3',5'-TRI-O-BENZOYLCYTIDINE
5'-O-METHOXYTRITYL-2'-O-ACETYLURIDINE-3'-CYANOETHYL(2,2,2-TRICHLOROETHYL)PHOSPHATE
N-BENZOYL-3',5'-DI-O-LEVULINYL-2'-O-(2-METHOXYETHYL)-5-METHYLCYTIDINE
Pentaacetyl-1-B-D-glucopyranosyl-cytosine
SJBRLUQFYTXRLT-UJCHZGTJSA-N
(2',3',4'-TRI-O-ACETYL-6'-O-TERT.-BUTYLDIMETHYLSILYL-BETA-D-GLUCOPYRANOSIDE)-THYMINE
| Title | Journal or Book | Year |
|---|---|---|
| Oligodeoxyribonucleotide Analogues with Bridging Dimethylene Sulfide, Sulfoxide, and Sulfone Groups. Toward a Second-Generation Model of Nucleic Acid Structure | The Journal of Organic Chemistry | 2002 |