Oligonucleotide Synthesis, RNA Raw Materials & Modification

Tetrabenzyl pyrophosphate

dibenzyl bis(phenylmethoxy)phosphoryl phosphate

제품 번호CH61002CAS 번호990-91-0순도99.5%
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제품 개요

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제품군
Oligonucleotide Synthesis, RNA Raw Materials & Modification
화학명
dibenzyl bis(phenylmethoxy)phosphoryl phosphate
분자식
C28H28O7P2
분자량
538.47
순도
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.

동의어

Tetrabenzyl pyrophosphate; Tetrabenzyl diphosphate; Pyrophosphoric acid tetrabenzyl ester; Diphosphoric acid tetrabenzyl ester; P,P,P',P'-Tetrakis(phenylmethyl) diphosphate; Benzyl pyrophosphate; Fosaprepitant Impurity S

식별 정보 및 규격

Catalog No.CH61002
CAS No.990-91-0
Molecular FormulaC28H28O7P2
Molecular Weight538.47
PubChem CID563183
InChIKeyNSBNXCZCLRBQTA-UHFFFAOYSA-N
Purity99.5%

보관 조건

Frozen below 0 C; under inert gas

기술 속성

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

응용 맥락

  • 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.

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