4-CHLORO-7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDINE
Compound with spectra: 2 NMR
![4-CHLORO-7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDINE](/api/compound/1Ik0dYiKLMv.png?ph=true&h=300&w=458 "4-CHLORO-7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDINE")
| SpectraBase Compound ID | 1Ik0dYiKLMv |
|---|---|
| InChI | InChI=1S/C11H11ClFN3O2/c12-10-6-1-2-16(11(6)15-5-14-10)9-3-7(13)8(4-17)18-9/h1-2,5,7-9,17H,3-4H2/t7-,8+,9+/m0/s1 |
| InChIKey | YYJLPTUBNDPPBD-DJLDLDEBSA-N |
| Mol Weight | 271.68 g/mol |
| Molecular Formula | C11H11ClFN3O2 |
| Exact Mass | 271.052382 g/mol |
| Enantiomer InChIKey | YYJLPTUBNDPPBD-VGMNWLOBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDIN-4-AMINE
7-(2-DEOXY-BETA-D-THREO-PENTOFURANOSYL)-2H-PYRROLO-[2,3-D]-PYRIMIDIN-4(3H)-ONE
4-AMINO-7-[2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSYL]-7H-PYRROLO-[2,3-D]-PYRIMIDINE
2-AMINO-4-CHLORO-7-(2,3-DIDEOXY-ALPHA-D-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDINE
1,7-DIDEAZA-2'-DEOXYADENOSINE
NUCLEOSIDE-#3A
2-AMINO-4-CHLORO-7-(2,3-DIDEOXY-BETA-D-GLYCERO-PENT-2-ENOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDINE
[6,7-15N]-2-Deoxyadenosine
9-[2',3'-DIDEOXY-3'-C-(HYDROXYMETHYL)-ALPHA-D-ERYTHROPENTOFURANOSYL]-ADENINE
9-[2',3'-DIDEOXY-3'-C-(HYDROXYMETHYL)-BETA-D-ERYTHROPENTOFURANOSYL]-ADENINE
| Title | Journal or Book | Year |
|---|---|---|
| 2′, 3′‐Dideoxy‐3′‐fluorotubercidin and Related Dideoxyribonucleosides:. Synthesis via a 2′‐deoxy‐3′‐oxoribofuranoside intermediate and conformation studies | Helvetica Chimica Acta | 1989 |