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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, 4,6-dichloro-2,5-dimethyl-

Cc1nc(Cl)c(c(n1)Cl)C Request for Quotation
Chemical Name: Pyrimidine, 4,6-dichloro-2,5-dimethyl-
CAS Number: 1780-33-2
Product Number: AG0025PU(AGN-PC-0JOD5P)
Synonyms:
MDL No:
Molecular Formula: C6H6Cl2N2
Molecular Weight: 177.0312

Identification/Properties

Computed Properties
Molecular Weight:
177.028g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
175.991g/mol
Monoisotopic Mass:
175.991g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,6-Dichloro-2,5-dimethylpyrimidine is a crucial intermediate in chemical synthesis, commonly utilized as a building block in various organic reactions. This compound serves as a versatile reagent in the pharmaceutical and agrochemical industries, playing a key role in the synthesis of complex molecules and active ingredients. Its unique structural properties make it particularly valuable in the development of pyrimidine-based drugs and pesticides. With its reactive nature and selective reactivity, 4,6-Dichloro-2,5-dimethylpyrimidine facilitates the formation of specific chemical bonds, enabling chemists to efficiently construct diverse molecular frameworks. This compound is renowned for its utility in the preparation of a wide range of biologically active compounds, highlighting its significance in chemical synthesis processes.