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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)-

4,5-dichloro-6-methyl-2-pyridin-2-ylpyrimidine

Cc1nc(nc(c1Cl)Cl)c1ccccn1 Request for Quotation
Chemical Name: 4,5-dichloro-6-methyl-2-pyridin-2-ylpyrimidine
CAS Number: 306935-55-7
Product Number: AG0030VH(AGN-PC-0KK7II)
Synonyms:
MDL No:
Molecular Formula: C10H7Cl2N3
Molecular Weight: 240.0887

Identification/Properties

Computed Properties
Molecular Weight:
240.087g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
239.002g/mol
Monoisotopic Mass:
239.002g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
215
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


4,5-Dichloro-6-methyl-2-(pyridin-2-yl)pyrimidine is a versatile compound widely used in chemical synthesis. Its unique molecular structure makes it a valuable building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as an important intermediate in the synthesis of pyrimidine-based drugs, such as antiviral and anticancer agents. Additionally, it is utilized in the development of novel materials and functional molecules with diverse applications in the fields of medicinal chemistry and materials science. The incorporation of 4,5-Dichloro-6-methyl-2-(pyridin-2-yl)pyrimidine in chemical reactions enables the efficient construction of complex molecular frameworks, offering opportunities for the creation of new therapeutic agents and advanced materials.