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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-chloro-4-methoxy-

COc1ccnc(n1)Cl Request for Quotation
Chemical Name: Pyrimidine, 2-chloro-4-methoxy-
CAS Number: 22536-63-6
Product Number: AG007OC5(AGN-PC-00LVYV)
Synonyms:
MDL No: MFCD00194055
Molecular Formula: C5H5ClN2O
Molecular Weight: 144.5590

Identification/Properties

Computed Properties
Molecular Weight:
144.558g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
144.009g/mol
Monoisotopic Mass:
144.009g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
91
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:
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-Chloro-4-methoxypyrimidine is a versatile chemical compound commonly used in chemical synthesis reactions. This compound serves as a valuable building block in the creation of a wide range of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it particularly useful in the production of complex organic molecules.2-Chloro-4-methoxypyrimidine is commonly employed as a nucleophilic substitution reagent, allowing chemists to introduce functional groups or modify existing ones in target molecules. It can react with various nucleophiles such as amines, alcohols, and thiols to form new bonds, enabling the creation of diverse chemical structures.Furthermore, 2-Chloro-4-methoxypyrimidine is frequently utilized in the synthesis of heterocyclic compounds due to its ability to participate in ring-forming reactions. By incorporating this compound into reactions, chemists can access a wide array of heterocycles with desired properties and functionalities.Overall, the application of 2-Chloro-4-methoxypyrimidine in chemical synthesis facilitates the efficient and strategic construction of complex organic molecules, making it an indispensable tool for synthetic chemists in the development of novel compounds for various industrial applications.