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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-dimethoxy-

COc1ncnc(c1)OC Request for Quotation
Chemical Name: Pyrimidine, 4,6-dimethoxy-
CAS Number: 5270-94-0
Product Number: AG003KJN(AGN-PC-0JNVNR)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O2
Molecular Weight: 140.1399

Identification/Properties

Properties
MP:
33 °C
BP:
186°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
140.142g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
140.059g/mol
Monoisotopic Mass:
140.059g/mol
Topological Polar Surface Area:
44.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.7
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-Dimethoxypyrimidine is a versatile chemical compound that finds widespread application in chemical synthesis processes. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals.In chemical synthesis, 4,6-Dimethoxypyrimidine acts as a valuable reagent for forming important carbon-carbon and carbon-heteroatom bonds. Its unique structure and reactivity allow for efficient functional group transformations and enable the synthesis of complex organic molecules.One of the primary uses of 4,6-Dimethoxypyrimidine is in the creation of pharmaceutical intermediates. By undergoing various chemical reactions, this compound can be transformed into key components of medications used to treat a wide range of medical conditions. Its role in drug synthesis highlights its significance in the pharmaceutical industry.Additionally, 4,6-Dimethoxypyrimidine is employed in the synthesis of agrochemicals, which are essential for crop protection and enhancing agricultural productivity. Through strategic chemical transformations, this compound contributes to the production of pesticides, herbicides, and fungicides that help safeguard crops from pests and diseases.Overall, the application of 4,6-Dimethoxypyrimidine in chemical synthesis underscores its importance as a versatile building block for creating valuable compounds across various industries.