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Catalog Number:
46153
CAS Number:
75999-66-5
2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride
Purity:
≥ 98% (GC)
Hazmat
Documents
$329.40 /5G
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Product Information

2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride is a versatile chemical compound known for its unique trifluoromethyl group, which enhances its reactivity and stability in various applications. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to introduce trifluoromethyl groups into organic molecules makes it particularly useful in medicinal chemistry, where such modifications can significantly influence the biological activity of drug candidates. Additionally, the presence of the methoxyphenyl group contributes to its solubility and compatibility with a range of solvents, facilitating its use in diverse chemical reactions.

Researchers and industry professionals can leverage 2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride for the development of novel compounds with enhanced properties. Its application in the synthesis of fluorinated compounds opens new avenues in drug discovery and material science, making it an essential tool for those looking to innovate in these fields. The compound's unique characteristics, such as its trifluoromethyl and methoxy functionalities, provide distinct advantages over similar compounds, allowing for more efficient and targeted synthesis processes.

CAS Number
75999-66-5
Purity
≥ 98% (GC)
Molecular Formula
C9H7ClF3NO
Molecular Weight
0
MDL Number
MFCD09030149
PubChem ID
10421682
Appearance
Light orange to yellow to green clear liquid
Boiling Point
98 °C/14 mmHg
Refractive Index
n20D 1.51
Conditions
Store at 2 - 8 °C
General Information
CAS Number
75999-66-5
Purity
≥ 98% (GC)
Molecular Formula
C9H7ClF3NO
Molecular Weight
0
MDL Number
MFCD09030149
PubChem ID
10421682
Appearance
Light orange to yellow to green clear liquid
Boiling Point
98 °C/14 mmHg
Refractive Index
n20D 1.51
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,2,2-Trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, contributing to the development of pesticides that are more effective against pests while being less harmful to beneficial insects.
  • Material Science: The compound is employed in creating advanced materials, such as polymers and coatings, which exhibit enhanced chemical resistance and durability, making them suitable for harsh environments.
  • Research Reagents: As a reagent in organic synthesis, it facilitates the creation of complex molecules, aiding researchers in the development of new compounds for various applications in chemistry and biology.
  • Fluorinated Compounds: Its unique trifluoromethyl group allows for the synthesis of fluorinated compounds, which are valuable in medicinal chemistry for improving the metabolic stability of drugs.

Citations