Amino-modified Nucleosides
2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine
Quick view. A protected 7-deaza nucleoside bearing 4-chloro, 5-iodo, N2-pivaloyl and 3',5'-di-O-(4-methylbenzoyl) features, CAS 199938-73-3. CAS 199938-73-3. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
Product profile
2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine is classified as amino-modified nucleosides (Formula C32H32ClIN4O6; molecular weight 730.98).
2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine provides a reactive functional group for conjugation, immobilization or linker-extension studies.
For 2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Names and search terms
Confirmed or normalized name variants
- GL102870
- CB04672397
Useful catalog search terms
- CAS 199938-73-3
- C32H32ClIN4O6
- PACUTHUGAMBGEU-RBZQAINGSA-N
- N2-pivaloyl 7-deaza nucleoside
- 4-chloro 5-iodo protected nucleoside
Physicochemical data
| Heterocycle | 7-Deaza pyrrolo[2,3-d]pyrimidine |
|---|---|
| Ring substituents | 4-Chloro and 5-iodo |
| Amino protection | N2-Pivaloyl |
| Sugar protection | 3',5'-Di-O-(4-methylbenzoyl) |
| Sugar state | 2'-Deoxy beta-D-ribofuranosyl |
| Stereochemistry | Three assigned sugar stereocenters |
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.
Product-specific evaluation notes
Potential advantages
- Reactive handles make the product adaptable across dye-labeling, surface-coupling and ligand-conjugation workflows.
Method limitations
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
These points describe 2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Frequently asked questions
Can the package size for 2-Amino-4-chloro-5-iodo-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine be customized?
Yes. Share the initial quantity, expected future scale, delivery timeline and packaging preference for review.
What information should be included in a quote request?
Quote catalog number BX-AMN-0039 and CAS 199938-73-3, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-family literature
These publications provide peer-reviewed context for the Amino-modified 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.
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.