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CAS 175137-27-6

:

methyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylate

Description:
Methyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features a chloro substituent at the 2-position and a trifluoromethyl group at the 4-position, contributing to its unique reactivity and properties. The carboxylate group at the 5-position, along with the methyl ester functionality, enhances its solubility in organic solvents and may influence its biological activity. The presence of the trifluoromethyl group typically imparts increased lipophilicity and can affect the compound's interaction with biological targets. Methyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylate is often utilized in medicinal chemistry and agrochemical applications due to its potential as a building block for the synthesis of more complex molecules. Its specific reactivity and stability can vary based on environmental conditions, making it a subject of interest in various chemical research fields.
Formula:C11H12ClF3N2O2
InChI:InChI=1/C11H12ClF3N2O2/c1-19-9(18)3-2-4-16-10-8(12)5-7(6-17-10)11(13,14)15/h5-6H,2-4H2,1H3,(H,16,17)
SMILES:COC(=O)CCCNc1c(cc(cn1)C(F)(F)F)Cl
Synonyms:
  • Methyl 4-{[3-Chloro-5-(Trifluoromethyl)Pyridin-2-Yl]Amino}Butanoate
  • 2-Chloro-4-Trifluoromethylprimidine-5-Carboxylate
  • 2-Chloro-4-trifluoromethyl-pyrimidine-5-carboxylicacid methyl ester
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