Silver(I) Trifluoromethanethiolate TCI S0977

Chemical Identity

CAS No.: 811-68-7
PubChem: CID 15972162·SID 354333285
Formula: CAgF3S
Molecular weight: 208.94 g/mol
Purity: >95.0%(T)
Reference databases: ChemSpider

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: silver trifluoromethanethiolate
SMILES: C(F)(F)(F)[S-].[Ag+]
InChIKey: GZRXLNQFRQGJLU-UHFFFAOYSA-M

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Silver(I) Trifluoromethanethiolate (TCI S0977), with CAS number 811-68-7, is a chemical compound widely used in laboratory settings for its catalytic properties. This compound is a silver(I) complex that plays a crucial role in various chemical reactions, particularly in catalysis and inorganic chemistry. Its unique structure allows it to interact effectively with different substrates, making it a valuable tool for researchers. It is commonly used in synthetic processes where high reactivity and specificity are required.

The compound is known for its strong electron-binding properties, which make it suitable for reactions involving electrophilic or nucleophilic interactions. Its ability to facilitate redox reactions and substitution processes makes it a preferred choice in both academic and industrial research. Due to its reactivity, it is often used in the synthesis of organic and inorganic compounds, contributing to the development of new materials and pharmaceuticals.

In Indonesian laboratories, Silver(I) Trifluoromethanethiolate is a key component in chemical research, especially in the fields of pure chemistry, material development, and pharmaceutical applications. Its sensitivity to moisture and oxidation requires careful handling, but its effectiveness in catalytic processes makes it an essential reagent for many scientific studies.

TCI brochures (PDF)

Trifluoromethylthiolation Reagents 2026-04-28 · p. 2
Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 9

Related TCI products

Catalytic Reactions: This compound is ideal for catalytic processes due to its high reactivity and ability to facilitate complex chemical transformations.
Redox Reactions: Its electron-binding properties make it suitable for redox reactions, where it can act as an oxidizing or reducing agent.
Organic Synthesis: It is commonly used in the synthesis of organic compounds, particularly in reactions requiring precise control over reaction pathways.
Inorganic Chemistry Research: Its role in inorganic chemistry allows it to be used in the development of new inorganic materials and compounds.
Pharmaceutical Development: It is utilized in the synthesis of pharmaceutical compounds, contributing to drug discovery and formulation processes.

From the TCI brochure

Conversion of alkyl-OH to alkyl-SCF3 with n-Bu4NI in toluene at 80°C

Brand	TCI
CAS number	811-68-7
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > Transition Elements
Pack sizes	Available in various quantities as per standard laboratory supply practices
Physical form	Solid or liquid, depending on the specific formulation
Storage	Should be stored in a dry, cool environment away from moisture and oxidizing agents

Silver(I) Trifluoromethanethiolate should be stored in a dry, cool location to prevent moisture-induced degradation. It is recommended to keep it in airtight containers to minimize exposure to air and humidity. Due to its sensitivity to oxidation, it should be stored away from strong oxidizing agents. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles. Regular monitoring of storage conditions ensures its stability and effectiveness. Proper labeling and secure storage are essential to prevent accidental exposure and maintain the integrity of the compound.

References cited in the TCI brochure

Jian‐Bo Liu. Direct Dehydroxytrifluoromethylthiolation of Alcohols Using Silver(I) Trifluoromethanethiolate and Tetra‐n‐butylammonium Iodide Angewandte Chemie International Edition, 2014. doi:10.1002/anie.201409983