(5-(TRIFLUOROMETHYL)PYRIMIDIN-2-YL)METHANOL|944905-41-3,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

(5-(TRIFLUOROMETHYL)PYRIMIDIN-2-YL)METHANOL

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Chemical Name:	(5-(TRIFLUOROMETHYL)PYRIMIDIN-2-YL)METHANOL
CAS Number:	944905-41-3
Product Number:	AG01DFB9(AGN-PC-0WAJX2)
Synonyms:
MDL No:
Molecular Formula:	C6H5F3N2O
Molecular Weight:	178.1119

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Chemical Structure

The (5-(Trifluoromethyl)pyrimidin-2-yl)methanol compound is a valuable tool in organic chemical synthesis as a versatile building block. Its unique structure containing a trifluoromethyl group attached to a pyrimidine ring confers distinctive properties that enhance its utility in creating novel molecules. This compound can be utilized as a starting material or intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its ability to introduce the trifluoromethyl functionality to target molecules. Additionally, the presence of the pyrimidine ring offers opportunities for further derivatization and modification, allowing for the synthesis of diverse chemical structures with potential biological or physicochemical activities. Overall, (5-(Trifluoromethyl)pyrimidin-2-yl)methanol serves as a valuable building block for designing and constructing complex molecules in chemical synthesis.