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Catalog Number:
45321
CAS Number:
583-02-8
Ethyl 4-(trifluoromethyl)benzoate
Purity:
≥ 98% (GC)
Synonym(s):
4-(Trifluoromethyl)benzoic acid ethyl ester
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Product Information

Ethyl 4-(trifluoromethyl)benzoate is a versatile compound known for its unique trifluoromethyl group, which enhances its chemical reactivity and stability. This compound is widely utilized in the synthesis of various pharmaceuticals and agrochemicals, making it an essential building block in the chemical industry. Its distinct properties allow it to serve as an effective intermediate in the production of fluorinated compounds, which are increasingly important in modern medicinal chemistry. Researchers appreciate its ability to improve the bioavailability and efficacy of drug formulations, while its application in crop protection products highlights its relevance in agricultural chemistry.

In addition to its role in synthesis, Ethyl 4-(trifluoromethyl)benzoate is recognized for its potential in developing new materials and fine chemicals. Its unique characteristics make it a valuable resource for professionals seeking to innovate in areas such as polymer science and specialty chemicals. With its favorable properties and broad applicability, this compound stands out as a key ingredient for advancing research and development across various sectors.

Synonyms
4-(Trifluoromethyl)benzoic acid ethyl ester
CAS Number
583-02-8
Purity
≥ 98% (GC)
Molecular Formula
C10H9F3O2
Molecular Weight
218.18
MDL Number
MFCD00013563
PubChem ID
521827
Density
1.24
Appearance
Colorless to almost colorless clear liquid
Boiling Point
80 °C/5 mmHg
Refractive Index
n20D 1.45
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-(Trifluoromethyl)benzoic acid ethyl ester
CAS Number
583-02-8
Purity
≥ 98% (GC)
Molecular Formula
C10H9F3O2
Molecular Weight
218.18
MDL Number
MFCD00013563
PubChem ID
521827
Density
1.24
Appearance
Colorless to almost colorless clear liquid
Boiling Point
80 °C/5 mmHg
Refractive Index
n20D 1.45
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 4-(trifluoromethyl)benzoate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of pharmaceuticals, particularly in creating compounds with enhanced biological activity due to the trifluoromethyl group, which can improve drug efficacy.
  • Agricultural Chemicals: It is used in formulating agrochemicals, including herbicides and pesticides, where its unique properties help in developing more effective and environmentally friendly solutions for crop protection.
  • Material Science: The compound finds applications in the production of specialty polymers and coatings that require enhanced chemical resistance and durability, making it valuable in industries like automotive and electronics.
  • Flavor and Fragrance Industry: Ethyl 4-(trifluoromethyl)benzoate is utilized in creating specific flavor and fragrance compounds, offering unique scent profiles that are appealing in consumer products.
  • Analytical Chemistry: It is employed as a standard in analytical methods, helping researchers in quantifying and identifying other chemical substances in complex mixtures, thus improving the accuracy of chemical analyses.

Citations