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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-chloro-6-methoxy-5-methylpyrimidine

COc1ncnc(c1C)Cl Request for Quotation
Chemical Name: 4-chloro-6-methoxy-5-methylpyrimidine
CAS Number: 960299-06-3
Product Number: AG00IJR5(AGN-PC-0D9FAB)
Synonyms:
MDL No:
Molecular Formula: C6H7ClN2O
Molecular Weight: 158.5856

Identification/Properties

Computed Properties
Molecular Weight:
158.585g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
158.025g/mol
Monoisotopic Mass:
158.025g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
112
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-Chloro-6-methoxy-5-methylpyrimidine, also known by its chemical formula C7H8ClN3O, is a valuable building block in chemical synthesis. This compound is commonly utilized in the production of various pharmaceuticals and agrochemicals due to its versatile properties and reactivity.In chemical synthesis, 4-Chloro-6-methoxy-5-methylpyrimidine serves as a key intermediate in the construction of complex organic molecules. It can undergo various reactions such as nucleophilic substitution, alkylation, and condensation reactions to introduce specific functional groups or modify its structure. This versatility makes it a crucial component in the creation of diverse compounds with important biological activities.Furthermore, the presence of the chloro, methoxy, and methyl groups in 4-Chloro-6-methoxy-5-methylpyrimidine provides opportunities for further derivatization, allowing chemists to tailor the molecule's properties according to the desired application. Its strategic placement of functional groups makes it a valuable tool for fine-tuning molecular structures in drug discovery, crop protection, and materials science.Overall, 4-Chloro-6-methoxy-5-methylpyrimidine plays a vital role in the field of chemical synthesis, enabling the efficient and precise construction of complex molecules with therapeutic, agricultural, and industrial relevance.