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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-methoxy-4,6-dimethyl-

COc1nc(C)cc(n1)C Request for Quotation
Chemical Name: Pyrimidine, 2-methoxy-4,6-dimethyl-
CAS Number: 14001-61-7
Product Number: AG001BXW(AGN-PC-008WWE)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O
Molecular Weight: 138.1671

Identification/Properties

Properties
MP:
34-70°C
BP:
234.1±43.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
138.17g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
138.079g/mol
Monoisotopic Mass:
138.079g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
97.8
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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-Methoxy-4,6-dimethylpyrimidine, also known as MDP, is a versatile compound that finds wide application in chemical synthesis processes. Its unique structure and properties make it a valuable building block in various industries.One of the key uses of 2-Methoxy-4,6-dimethylpyrimidine is as a reagent in organic chemistry reactions. It serves as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and other specialty chemicals. Its structure allows for selective functional group transformations, making it a valuable tool in the creation of complex molecules.In particular, 2-Methoxy-4,6-dimethylpyrimidine is commonly employed in the construction of heterocyclic structures due to its ability to participate in ring-forming reactions. It can act as a precursor for the production of pyrimidine derivatives with diverse functionalities, contributing to the development of new materials and compounds with potential applications in drug discovery and materials science.Furthermore, 2-Methoxy-4,6-dimethylpyrimidine's compatibility with various reaction conditions and its stability make it a preferred choice in chemical synthesis. Its ease of handling and storage further enhances its utility in laboratory and industrial settings.Overall, 2-Methoxy-4,6-dimethylpyrimidine plays a crucial role in expanding the synthetic possibilities in organic chemistry, enabling the efficient production of valuable compounds for a range of applications.