1. Home
  2. 6-TRIFLUOROMETHYL-PYRIMIDINE-4-CARBOXYLIC ACID

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

6-TRIFLUOROMETHYL-PYRIMIDINE-4-CARBOXYLIC ACID

OC(=O)c1ncnc(c1)C(F)(F)F Request for Quotation
Chemical Name: 6-TRIFLUOROMETHYL-PYRIMIDINE-4-CARBOXYLIC ACID
CAS Number: 933721-99-4
Product Number: AG0063OR(AGN-PC-0WNVTJ)
Synonyms:
MDL No:
Molecular Formula: C6H3F3N2O2
Molecular Weight: 192.0954

Identification/Properties

Properties
BP:
294.4±40.0 °C(Predicted)
Form:
Solid
Computed Properties
Molecular Weight:
192.097g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
1
Exact Mass:
192.015g/mol
Monoisotopic Mass:
192.015g/mol
Topological Polar Surface Area:
63.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
207
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The 6-(Trifluoromethyl)pyrimidine-4-carboxylic acid is a versatile compound commonly utilized in a variety of chemical synthesis reactions. This compound is valued for its ability to serve as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. When utilized in chemical synthesis, 6-(Trifluoromethyl)pyrimidine-4-carboxylic acid can act as a precursor for the introduction of the trifluoromethyl group into organic molecules, enhancing their bioactivity, stability, and overall properties. Its unique structure facilitates the formation of novel molecular structures through diverse synthetic routes, making it a valuable tool for organic chemists in the creation of complex and valuable compounds.