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Catalog Number:
46477
CAS Number:
64035-64-9
Trifluorometanosulfonato de (trimetilsilil)metilo [Reactivo de metilación de trimetilsilil]
Purity:
≥ 98% (GC)
Synonym(s):
Éster metílico del ácido trifluorometanosulfónico (trimetilsilil), Triflato de (trimetilsilil)metilo
Hazmat
Documents
$69.90 /1G
Tamaño
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Product Information

(Trimethylsilyl)methyl trifluoromethanesulfonate, commonly known as Trimethylsilylmethylating Reagent, is a versatile chemical compound widely utilized in organic synthesis and medicinal chemistry. This reagent is particularly valued for its ability to introduce trimethylsilylmethyl groups into various substrates, enhancing their reactivity and stability. Its unique trifluoromethanesulfonate moiety provides excellent leaving group properties, making it an ideal choice for nucleophilic substitution reactions. Researchers and industry professionals leverage this compound for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, where precise functionalization is crucial.

The compound's efficiency in facilitating the formation of carbon-silicon bonds opens new pathways in the development of silicon-containing materials, which are increasingly important in electronics and materials science. Its compatibility with a wide range of functional groups further enhances its utility in diverse applications, making it a valuable tool for chemists seeking to optimize their synthetic routes. With its ability to streamline processes and improve yields, (Trimethylsilyl)methyl trifluoromethanesulfonate stands out as a key reagent in modern chemical research and development.

Synonyms
Éster metílico del ácido trifluorometanosulfónico (trimetilsilil), Triflato de (trimetilsilil)metilo
CAS Number
64035-64-9
Purity
≥ 98% (GC)
Molecular Formula
C5H11F3O3SSi
Molecular Weight
236.28
MDL Number
MFCD00009914
PubChem ID
2760857
Density
1.19
Appearance
Líquido transparente incoloro a amarillo claro.
Boiling Point
168 °C
Refractive Index
n20D 1,38
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éster metílico del ácido trifluorometanosulfónico (trimetilsilil), Triflato de (trimetilsilil)metilo
CAS Number
64035-64-9
Purity
≥ 98% (GC)
Molecular Formula
C5H11F3O3SSi
Molecular Weight
236.28
MDL Number
MFCD00009914
PubChem ID
2760857
Density
1.19
Appearance
Líquido transparente incoloro a amarillo claro.
Boiling Point
168 °C
Refractive Index
n20D 1,38
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(Trimethylsilyl)methyl trifluoromethanesulfonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a powerful methylating agent, enabling chemists to introduce methyl groups into various organic molecules, which is essential for synthesizing pharmaceuticals and agrochemicals.
  • Protecting Group Chemistry: It acts as a protecting group for alcohols and amines, allowing for selective reactions without interference from these functional groups, which is crucial in multi-step synthesis processes.
  • Fluorinated Compound Development: The trifluoromethanesulfonate moiety enhances the reactivity of the compound, making it valuable in developing fluorinated compounds that are important in medicinal chemistry and materials science.
  • Polymer Chemistry: It can be used in the modification of polymers, improving their properties and functionalities, which is beneficial in industries such as coatings, adhesives, and sealants.
  • Analytical Chemistry: This reagent is useful in derivatization techniques for analytical methods, enhancing the detection and quantification of various compounds in complex mixtures.

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