Tetrabenzyl pyrophosphate
dibenzyl bis(phenylmethoxy)phosphoryl phosphate
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- Nom chimique
- dibenzyl bis(phenylmethoxy)phosphoryl phosphate
- FM
- C28H28O7P2
- PM
- 538.47
- Pureté
- 99.5%
Tetrabenzyl pyrophosphate is a protected pyrophosphate reagent also indexed as tetrabenzyl diphosphate, pyrophosphoric acid tetrabenzyl ester, diphosphoric acid tetrabenzyl ester, and benzyl pyrophosphate.
CH61002 is listed with CAS 990-91-0, molecular formula C28H28O7P2, and molecular weight 538.47. Research literature links tetrabenzyl pyrophosphate with chemoselective phosphorylation, phosphate synthesis, phosphodiester and phosphoramidate library workflows, protected glycosyl phosphate linkage formation, nucleotide-sugar derivative synthesis, and lead-ion responsive neutral-carrier research.
Synonymes
Tetrabenzyl pyrophosphate; Tetrabenzyl diphosphate; Pyrophosphoric acid tetrabenzyl ester; Diphosphoric acid tetrabenzyl ester; P,P,P',P'-Tetrakis(phenylmethyl) diphosphate; Benzyl pyrophosphate; Fosaprepitant Impurity S
Identité et spécifications
| Catalog No. | CH61002 |
| CAS No. | 990-91-0 |
| Molecular Formula | C28H28O7P2 |
| Molecular Weight | 538.47 |
| PubChem CID | 563183 |
| InChIKey | NSBNXCZCLRBQTA-UHFFFAOYSA-N |
| Purity | 99.5% |
Conditions de stockage
Frozen below 0 C; under inert gas
Caractéristiques techniques
- Reagent class
- Protected pyrophosphate
- Phosphate protection
- Tetrabenzyl
- Phosphorus motif
- Pyrophosphate (P-O-P)
- Supported synthesis role
- Chemoselective phosphorylation reagent
- Packaging
- 1 g glass bottle with plastic insert; 100 kg batch; Custom packaging on request
- Water content
- Specification <=0.5%; result 0.12%
- Physical form
- Solid
- Stability
- Produced 2024-02-20; expiry 2026-02-20
Contexte d’application
- Phosphate synthesis: reported as a protected pyrophosphate reagent in chemoselective phosphorylation and debenzylation workflows.
- Phosphodiester and phosphoramidate workflows: reported in late-stage divergent synthesis of phosphodiester and phosphoramidate libraries.
- Glycosyl phosphate and nucleotide-sugar chemistry: aligned with protected glycosyl phosphate linkage formation and cytidine-diphosphate sugar derivative synthesis.
- Lead-ion carrier research: reported as a neutral carrier responsive to lead ion in analytical chemistry research.
Ressources techniques associées
Sources publiques
- Sustainability Challenges and Opportunities in Oligonucleotide Manufacturing
Journal of Organic Chemistry, 2021
Product-family technical context
- Solid-phase supports for oligonucleotide synthesis
Current Protocols in Nucleic Acid Chemistry, 2013
Product-family technical context
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Tetrahedron Letters, 1981
Product-family technical context
- Synthesis of deoxyoligonucleotides on a polymer support
Journal of the American Chemical Society, 1981
Product-family technical context
- Composé PubChem 563183
PubChem · CID 563183
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