It functions as a precursor to a Wittig reagent that enables carbon–carbon double bond formation through an olefination reaction with a suitable carbonyl compound. This reaction helps build an important structural fragment required for the molecule. After this step, the product undergoes further chemical transformations such as reduction, substitution, or deprotection steps during the manufacturing process, ultimately leading to the formation of the final Active Pharmaceutical Ingredient. (Methoxymethyl)triphenylphosphonium chloride serves as a synthetic reagent in the preparation of Tofacitinib.
(Methoxymethyl)triphenylphosphonium chloride
| CAS No | 4009-98-7 |
|---|---|
| Molecular Formula | C20H20OP+ |
| Molecular Weight | 307.3 g/mol |
| Synonyms | methoxymethyl(triphenyl)phosphanium |
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Frequently Asked Questions
It functions as a precursor to a Wittig reagent that enables carbon–carbon double bond formation through an olefination reaction with a suitable carbonyl compound. This reaction helps build an important structural fragment required for the molecule. After this step, the product undergoes further chemical transformations such as reduction, substitution, or deprotection steps during the manufacturing process, ultimately leading to the formation of the final Active Pharmaceutical Ingredient. (Methoxymethyl)triphenylphosphonium chloride serves as a synthetic reagent in the preparation of Tofacitinib.
The CAS number of (Methoxymethyl)triphenylphosphonium chloride is 4009-98-7.
The molecular formula of (Methoxymethyl)triphenylphosphonium chloride is C20H20OP+.
The listed molecular weight of (Methoxymethyl)triphenylphosphonium chloride is 307.3 g/mol.
The listed synonym or IUPAC name for (Methoxymethyl)triphenylphosphonium chloride is methoxymethyl(triphenyl)phosphanium.