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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)-

5-Pyrimidinamine, 2-chloro-4-methoxy-

COc1nc(Cl)ncc1N Request for Quotation
Chemical Name: 5-Pyrimidinamine, 2-chloro-4-methoxy-
CAS Number: 96833-41-9
Product Number: AG00IJV6(AGN-PC-0379Y5)
Synonyms:
MDL No: MFCD12402341
Molecular Formula: C5H6ClN3O
Molecular Weight: 159.5736

Identification/Properties

Computed Properties
Molecular Weight:
159.573g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
159.02g/mol
Monoisotopic Mass:
159.02g/mol
Topological Polar Surface Area:
61A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
113
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


2-Chloro-4-methoxypyrimidin-5-amine, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals.In chemical synthesis, 2-Chloro-4-methoxypyrimidin-5-amine can be employed as a key intermediate in the production of biologically active molecules. Its unique structure and functional groups allow for the introduction of specific substituents, enabling the modification of the compound to generate a wide range of derivatives with different properties and applications.Furthermore, the presence of the chloro and methoxy groups in the molecule imparts distinct reactivity, facilitating selective reactions and structural transformations in synthetic pathways. This versatility makes 2-Chloro-4-methoxypyrimidin-5-amine a valuable tool for organic chemists and researchers seeking to design and create novel compounds with desired characteristics.Overall, the application of 2-Chloro-4-methoxypyrimidin-5-amine in chemical synthesis enables the efficient and strategic construction of complex molecules, ultimately contributing to the development of new drugs, agricultural chemicals, and other innovative products in the field of chemistry.