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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)-

Pyrimidine, 2,4,5-trichloro-6-(trifluoromethyl)-

Clc1nc(Cl)c(c(n1)C(F)(F)F)Cl Request for Quotation
Chemical Name: Pyrimidine, 2,4,5-trichloro-6-(trifluoromethyl)-
CAS Number: 84737-23-5
Product Number: AG004SA5(AGN-PC-0JM8RZ)
Synonyms:
MDL No:
Molecular Formula: C5Cl3F3N2
Molecular Weight: 251.4211

Identification/Properties

Properties
BP:
254.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

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


2,4,5-Trichloro-6-(trifluoromethyl)pyrimidine is a highly versatile compound that finds extensive application in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique chemical properties.In chemical synthesis, 2,4,5-Trichloro-6-(trifluoromethyl)pyrimidine is often utilized as a reagent for introducing the trifluoromethyl group into organic molecules. The trifluoromethyl group is known for its electron-withdrawing nature, making it a valuable moiety in the design of bioactive compounds with enhanced pharmacological properties.Furthermore, the trichloro substituents on the pyrimidine ring provide significant synthetic versatility, allowing for further functionalization through various chemical reactions. This compound is particularly valuable in the development of novel drug candidates, as the trifluoromethyl group can improve the metabolic stability, lipophilicity, and overall potency of the resulting molecules.Overall, 2,4,5-Trichloro-6-(trifluoromethyl)pyrimidine plays a crucial role in modern chemical synthesis by enabling the construction of complex molecular structures with enhanced biological activities for potential applications in the pharmaceutical and agrochemical industries.