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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-chloro-2-methoxy-6-(trifluoromethyl)pyrimidine

COc1nc(Cl)cc(n1)C(F)(F)F Request for Quotation
Chemical Name: 4-chloro-2-methoxy-6-(trifluoromethyl)pyrimidine
CAS Number: 932701-90-1
Product Number: AG00IHIQ(AGN-PC-0BSHBZ)
Synonyms:
MDL No:
Molecular Formula: C6H4ClF3N2O
Molecular Weight: 212.5569696

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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-Chloro-2-methoxy-6-(trifluoromethyl)pyrimidine is a versatile compound frequently employed in chemical synthesis for its unique reactivity and structural properties. Its ability to participate in various synthetic transformations makes it a valuable building block in the creation of a wide range of organic compounds. One notable application of this compound is as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. By serving as a crucial starting material, 4-Chloro-2-methoxy-6-(trifluoromethyl)pyrimidine enables chemists to access complex molecular structures with strategic control over regioselectivity and functional group compatibility. Furthermore, its trifluoromethyl substituent imparts enhanced lipophilicity and bioactivity to the final products, making it particularly beneficial in drug discovery and development efforts. Additionally, the presence of the chloro and methoxy groups on the pyrimidine scaffold further expand the synthetic versatility of this compound, allowing for the introduction of additional functionalities through straightforward chemical manipulations. Overall, the utility of 4-Chloro-2-methoxy-6-(trifluoromethyl)pyrimidine in chemical synthesis underscores its importance as a valuable tool in the modern organic chemist's arsenal.