Methyl triflate, >98%
Price range: $342.00 through $2,958.00
Product Code: KI-0002-HPCAS NO: 333-27-7
- Chemical Formula: C2H3F3O3S
- Synonyms: MeOTf, Methyl trifluoromethanesulfonate, Trifluoromethanesulfonic acid methyl ester
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SUM Formula: C2H3F3O3S
Molecular Weight: 164.10
Purity: >98%
- SUM Formula: C2H3F3O3S
- Molecular Weight: 164.10
Methyl triflate, CAS: 333-27-7
Key Applications:
1. Organic Synthesis & Methylation Chemistry
- Highโreactivity methylating agent for oxygen, nitrogen, sulfur, and carbon nucleophiles.
- Enables Oโmethylation of alcohols and phenols, Nโmethylation of amines and heterocycles, and Sโmethylation of thiols.
- Frequently used when milder methylating agents (e.g., dimethyl sulfate, methyl iodide) are insufficient.
2. Pharmaceutical & Fine Chemical Intermediates
- Supports the synthesis of API intermediates, heterocycles, and alkaloid derivatives.
- Used in lateโstage functionalization where high selectivity and strong electrophilicity are required.
- Plays a role in constructing quaternary ammonium salts and cationic building blocks.
3. Catalyst Activation & Salt Formation
- Converts neutral ligands or precatalysts into cationic, highly active catalytic species.
- Commonly used to generate cationic metal complexes in:
- CโH activation
- Olefin polymerization
- Crossโcoupling catalysis
4. Materials Science & Polymer Chemistry
- Methylates functional groups in specialty polymers, enabling:
- Chargeโtransport tuning
- Ionโexchange membrane modification
- Surface functionalization for advanced materials
5. Ionic Liquid & Salt Synthesis
- Key reagent for preparing methylated cations, including:
- Quaternary ammonium salts
- Phosphonium salts
- Sulfonium salts
- Supports the development of taskโspecific ionic liquids with tailored polarity and conductivity.
6. Protecting Group Chemistry
- Used to install methyl protecting groups on nucleophilic sites.
- Offers high yields and clean reaction profiles, especially in complex molecule synthesis.
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