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Catalog Number:
27703
CAS Number:
149771-09-5
Ethyl 2-amino-4-(trifluoromethyl)pyrimidine-5-carboxylate
Purity:
≥ 99% (HPLC)
Documents
$37.96 /1G
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Product Information

Ethyl 2-amino-4-(trifluoromethyl)pyrimidine-5-carboxylate is a versatile compound recognized for its unique trifluoromethyl group, which enhances its biological activity and chemical stability. This compound is particularly valuable in pharmaceutical research, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its ability to modify the pharmacokinetic properties of drug candidates makes it an essential building block in the development of novel therapeutics, especially in the fields of oncology and infectious diseases.

Moreover, Ethyl 2-amino-4-(trifluoromethyl)pyrimidine-5-carboxylate is utilized in agrochemical formulations, contributing to the development of advanced crop protection agents. Its distinctive properties allow for improved efficacy and selectivity in pest control applications. Researchers and industry professionals can leverage this compound to enhance product performance while minimizing environmental impact, making it an attractive option for sustainable agricultural practices.

CAS Number
149771-09-5
Purity
≥ 99% (HPLC)
Molecular Formula
C8H8F3N3O2
Molecular Weight
235.16
MDL Number
MFCD00052070
PubChem ID
2737153
Melting Point
181 - 184 ?C
Appearance
White crystalline solid
Conditions
Store at 0-8°C
General Information
CAS Number
149771-09-5
Purity
≥ 99% (HPLC)
Molecular Formula
C8H8F3N3O2
Molecular Weight
235.16
MDL Number
MFCD00052070
PubChem ID
2737153
Melting Point
181 - 184 ?C
Appearance
White crystalline solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 2-amino-4-(trifluoromethyl)pyrimidine-5-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its unique trifluoromethyl group which enhances bioactivity.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing effective solutions for pest control and crop protection, thereby improving agricultural productivity.
  • Material Science: The compound is explored for its potential in developing advanced materials, particularly in coatings and polymers, where its properties can enhance durability and resistance to environmental factors.
  • Biochemical Research: Researchers utilize this chemical in studies related to enzyme inhibition and receptor binding, contributing to a better understanding of biological processes and disease mechanisms.
  • Fluorinated Compound Synthesis: Its ability to introduce trifluoromethyl groups makes it valuable in synthesizing other fluorinated compounds, which are important in various industrial applications, including pharmaceuticals and specialty chemicals.

Citations