CAS NO:137218-25-8 2-(2-(Trifluoromethoxy)phenyl)acetonitrile
CAS NO:137218-25-8 NAME:2-(2-(Trifluoromethoxy)phenyl)acetonitrile MF：C9H6F3NO MW：201.15 EINECS：642-508-0 PURITY:97%MIN APPEARANCE:Colorless to Light yellow powder to crystal COA:Provide Sample:Negotiable
Categories：
Material Chemistry
Other Material Chemicals
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Product introduction
| PRODUCT NAME | 2-(2-(Trifluoromethoxy)phenyl)acetonitrile |
| CAS NO | 137218-25-8 |
| FP | >230 °F |
| BP | 222-223 °C(lit.) |
| DENSITY | 1.28 g/mL at 25 °C(lit.) |
| STORAGE | Sealed in dry,Room Temperature |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of CAS NO:137218-25-8 2-(2-(Trifluoromethoxy)phenyl)acetonitrile
2-(Trifluoromethoxy)phenylacetonitrile CAS NO:137218-25-8 is a compound that features a trifluoromethyl group attached to a phenyl ring, which is further linked to an acetonitrile group. This structure is of interest due to the unique properties imparted by the trifluoromethyl group, such as increased lipophilicity and metabolic stability, making it a valuable moiety in medicinal chemistry and materials science.
Applications of CAS NO:137218-25-8 2-(2-(Trifluoromethoxy)phenyl)acetonitrile
1)Reactivity and Characterization
2-(Trifluoromethoxy)phenylacetonitrile exhibits unique reactivity, such as the loss of fluorine atoms, leading to the formation of trimeric compounds.
2)Synthesis Applications
It plays a crucial role in trifluoromethoxylation reactions. For instance, it's used in generating trifluoromethoxide anions to substitute activated bromides, leading to the formation of aliphatic trifluoromethyl ethers
3)Spectroscopic Studies
The compound has been extensively studied using Fourier transform infrared (FT-IR) and Fourier transform Raman (FT-Raman) spectroscopy. These studies provide insights into the molecule's structural and electronic properties, including charge transfer interactions
4)Catalysis and Synthetic Chemistry
It's used in asymmetric silver-catalysed intermolecular bromotrifluoromethoxylation of alkenes, an important process in pharmaceuticals and agrochemicals due to the strong electron-withdrawing nature and high lipophilicity of trifluoromethoxy groups
5)Chemical Transformation and Reactions
The compound is involved in novel chemical transformations, such as the chemoselective cyclization of alkynyl nitriles, which has significant implications in organic synthesis
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