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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)-

4-(chloromethyl)-6-(trifluoromethyl)pyrimidine

ClCc1ncnc(c1)C(F)(F)F Request for Quotation
Chemical Name: 4-(chloromethyl)-6-(trifluoromethyl)pyrimidine
CAS Number: 944901-47-7
Product Number: AG006AB6(AGN-PC-0ALQL8)
Synonyms:
MDL No:
Molecular Formula: C6H4ClF3N2
Molecular Weight: 196.5576

Identification/Properties

Properties
BP:
210.7±35.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Chloromethyl)-6-(trifluoromethyl)pyrimidine is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional group compatibility. As a key intermediate in organic chemistry, it serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and materials.One of the prominent applications of 4-(Chloromethyl)-6-(trifluoromethyl)pyrimidine is in the construction of heterocyclic compounds through versatile functional group transformations. Its chlorine and trifluoromethyl groups serve as important reactive handles for further derivatization, enabling the introduction of diverse substituents at these positions. This reactivity opens up a wide range of synthetic possibilities, making it a valuable tool in the preparation of complex molecular structures.Moreover, the presence of both electron-withdrawing and electron-donating substituents in 4-(Chloromethyl)-6-(trifluoromethyl)pyrimidine confers enhanced stability and reactivity to the compound, allowing for efficient and selective reactions in various synthetic pathways. Its compatibility with a variety of reaction conditions and functional groups makes it a versatile reagent for the synthesis of target molecules with specific functionalities.Overall, the strategic incorporation of 4-(Chloromethyl)-6-(trifluoromethyl)pyrimidine in chemical synthesis offers synthetic chemists a powerful tool for the efficient assembly of structurally diverse and complex molecules, facilitating the development of novel pharmaceuticals, agrochemicals, and materials.