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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)-

1,3,5-Triazine-2,4-diamine, N-[3-(trifluoromethyl)phenyl]-

Nc1ncnc(n1)Nc1cccc(c1)C(F)(F)F Request for Quotation
Chemical Name: 1,3,5-Triazine-2,4-diamine, N-[3-(trifluoromethyl)phenyl]-
CAS Number: 3832-69-7
Product Number: AG00CZYX(AGN-PC-0JV6XX)
Synonyms:
MDL No:
Molecular Formula: C10H8F3N5
Molecular Weight: 255.1992

Identification/Properties

Computed Properties
Molecular Weight:
255.204g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
2
Exact Mass:
255.073g/mol
Monoisotopic Mass:
255.073g/mol
Topological Polar Surface Area:
76.7A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
273
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound N2-(3-(Trifluoromethyl)phenyl)-1,3,5-triazine-2,4-diamine is commonly used in chemical synthesis as a versatile building block for creating various functional organic molecules. With its unique structure and properties, this compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials.In organic synthesis, N2-(3-(Trifluoromethyl)phenyl)-1,3,5-triazine-2,4-diamine can participate in a range of reactions such as cross-coupling, cyclization, and nucleophilic substitution. Its trifluoromethylphenyl group enhances the compound's reactivity and stability, making it a valuable tool in building complex molecular structures with high efficiency.Furthermore, the triazine core of this compound offers multiple sites for functionalization, allowing for precise modifications to tailor the molecule for specific applications. This versatility makes N2-(3-(Trifluoromethyl)phenyl)-1,3,5-triazine-2,4-diamine an essential component in the toolkit of synthetic chemists working in the fields of drug discovery, material science, and chemical biology.Through strategic use of N2-(3-(Trifluoromethyl)phenyl)-1,3,5-triazine-2,4-diamine in chemical synthesis, researchers can access new and innovative compounds with diverse properties and potential therapeutic or industrial applications.