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Trifluorophenylsilane

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Identification
Molecular formula
C6H5F3Si
CAS number
13833-36-4
IUPAC name
trifluoro(phenyl)silane
State
State

At room temperature, trifluorophenylsilane is in a liquid state.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
143.00
Boiling point (Kelvin)
416.15
General information
Molecular weight
176.19g/mol
Molar mass
176.1860g/mol
Density
1.2330g/cm3
Appearence

Trifluorophenylsilane appears as a colorless liquid.

Comment on solubility

Solubility of Trifluoro(phenyl)silane

Trifluoro(phenyl)silane, with the chemical formula C6H4F3Si, exhibits unique solubility characteristics that are important for its use in various chemical applications.

When considering its solubility, it is essential to note the following:

  • Polarity: Trifluoro(phenyl)silane features a polar trifluoromethyl group that can affect its interaction with different solvents.
  • Solvent Compatibility: It is generally more soluble in non-polar solvents such as aromatic hydrocarbons (e.g., toluene, benzene) due to its phenyl group, while its solubility in polar solvents like water is very low.
  • Temperature Influence: Like many chemical compounds, its solubility can increase with temperature, suggesting that higher temperatures might facilitate greater dissolution in compatible solvents.

In summary, understanding the solubility of trifluoro(phenyl)silane is crucial for its practical applications, particularly in fields that utilize silane coupling agents. Its potency as a silane reagent arises partly from its solvable nature in the right environments, making it a valuable compound in synthetic pathways.

Interesting facts

Interesting Facts about Trifluoro(phenyl)silane

Trifluoro(phenyl)silane is an intriguing chemical compound that belongs to the category of organosilicon compounds. This versatile compound is known for its unique properties and is widely studied for various applications in chemistry. Here are some fascinating insights into trifluoro(phenyl)silane:

  • Structure and Bonding: The presence of the Si-F bonds in trifluoro(phenyl)silane contributes to its stability and reactivity. The trifluoromethyl group effectively alters the electronic properties of the molecule, making it a valuable precursor in various reactions.
  • Applications in Material Science: Trifluoro(phenyl)silane is often utilized in material science, particularly in the synthesis of advanced polymers and coatings. Its fluorinated groups enhance the durability and chemical resistance of the resulting materials.
  • Silicon-Based Chemistry: The compound serves as a building block in silicon-based chemistry, enabling the formation of complex siloxane networks. This is particularly useful in developing compounds with tailored properties for specific applications.
  • Role in Electronics: Due to its ability to modify surface chemistry, trifluoro(phenyl)silane finds applications in the semiconductor industry. It is employed in the fabrication of thin films and as a surface modifier to improve adhesion and electrical properties.
  • Research and Development: Ongoing research into trifluoro(phenyl)silane focuses on exploring its potential in catalysis and as a functional additive in various chemical reactions. Its fluorine atoms often facilitate unique reaction pathways that are not achievable with simpler silanes.

In summary, trifluoro(phenyl)silane exemplifies the significance of organosilicon compounds in modern chemistry and material science. As we continue to explore its properties and applications, it offers exciting possibilities for innovative technological advancements.

Synonyms
Phenyltrifluorosilane
368-47-8
trifluoro(phenyl)silane
Benzene,(trifluorosilyl)-
SILANE, PHENYLTRIFLUORO-
Phenyl trifluorosilane
G9KX9P6ZV4
Fenyl-trifluorsilan
Fenyl-trifluorsilan [Czech]
Trifluorophenylsilane
BRN 2935897
trifluorophenyl silane
MFCD00054907
trifluoro-phenyl-silane
UNII-G9KX9P6ZV4
SCHEMBL49748
4-16-00-01559 (Beilstein Handbook Reference)
KGWNTHHPMKEAIK-UHFFFAOYSA-
DTXSID90190267
AKOS006228440
FS-6343
DB-321397
CS-0207367
S13725
InChI=1/C6H5F3Si/c7-10(8,9)6-4-2-1-3-5-6/h1-5H