Halogenated Nucleosides
N4-Benzoyl-2'-deoxy-5-iodocytidine
Quick view. An N4-benzoyl-protected 5-iodo-2'-deoxycytidine building block for structure-specific nucleoside and nucleotide synthesis research. CAS 158042-39-8. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Product profile
N4-Benzoyl-2'-deoxy-5-iodocytidine is classified as halogenated nucleosides (Formula C16H16IN3O5; molecular weight 457.22).
N4-Benzoyl-2'-deoxy-5-iodocytidine — N4-benzoyl-protected 5-iodo-2'-deoxycytidine building block for structure-specific nucleoside and nucleotide synthesis research.
For N4-Benzoyl-2'-deoxy-5-iodocytidine, confirm the current specification, storage conditions and downstream-method compatibility before routine use.
Names and search terms
Useful catalog search terms
- CAS 158042-39-8
- PubChem CID 91827922
Physicochemical data
| PubChem CID | 91827922 |
|---|---|
| InChIKey | NIHRRVGTTLNUQZ-YNEHKIRRSA-N |
| IUPAC name | N-[1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-2-oxopyrimidin-4-yl]benzamide |
| SMILES | C1[C@@H]([C@H](O[C@H]1N2C=C(C(=NC2=O)NC(=O)C3=CC=CC=C3)I)CO)O |
| Sugar modification | 2'-deoxy |
| Nucleobase modification | 5-iodo |
| Protecting group | N4-benzoyl |
| InChI | InChI=1S/C16H16IN3O5/c17-10-7-20(13-6-11(22)12(8-21)25-13)16(24)19-14(10)18-15(23)9-4-2-1-3-5-9/h1-5,7,11-13,21-22H,6,8H2,(H,18,19,23,24)/t11-,12+,13+/m0/s1 |
Release documentation
The current specification defines the analytical method and acceptance criteria; the released lot result is reported on the CoA.
Additional HPLC, MS or NMR documentation can be agreed during technical review where available.
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Product-family literature
These publications provide peer-reviewed context for the Halogenated Nucleosides product family and its named chemistry. They are background reading only, not evidence for the exact product, supplied form, lot specification, availability or performance.
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