Amino-modified Nucleosides
2-Amino-4-chloro-N2-pivaloyl-7-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-beta-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine
Quick view. A protected 2-amino-4-chloro-7-deazapurine 2'-deoxynucleoside bearing N2-pivaloyl and 3',5'-di-O-(4-methylbenzoyl) groups, CAS 1878120-03-6. CAS 1878120-03-6. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
Product profile
2-Amino-4-chloro-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 C32H33ClN4O6; molecular weight 605.08).
2-Amino-4-chloro-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-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
- N-[4-chloro-7-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-beta-D-erythro-pentofuranosyl]-7H-pyrrolo[2,3-d]pyrimidin-2-yl]-2,2-dimethylpropanamide
- GL102869
Useful catalog search terms
- CAS 1878120-03-6
- C32H33ClN4O6
- DFSHVGUBFHFJHZ-ISJGIBHGSA-N
- N2-pivaloyl 7-deazapurine nucleoside
Physicochemical data
| Heterocycle | 2-Amino-4-chloro-7H-pyrrolo[2,3-d]pyrimidine |
|---|---|
| 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-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-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-0038 and CAS 1878120-03-6, 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.