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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-bromo-2-methoxypyrimidin-4-amine

COc1ncc(c(n1)N)Br Request for Quotation
Chemical Name: 5-bromo-2-methoxypyrimidin-4-amine
CAS Number: 148214-56-6
Product Number: AG001FIT(AGN-PC-07HAYH)
Synonyms:
MDL No:
Molecular Formula: C5H6BrN3O
Molecular Weight: 204.0246

Identification/Properties

Computed Properties
Molecular Weight:
204.027g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
202.969g/mol
Monoisotopic Mass:
202.969g/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


5-Bromo-2-methoxypyrimidin-4-amine is a versatile chemical compound commonly used in chemical synthesis as a crucial building block for the creation of various pharmaceuticals and agrochemicals. This compound serves as a key intermediate in the synthesis of potent bioactive molecules due to its unique structure and reactivity.The presence of the bromo group at the 5-position and the methoxy group at the 2-position of the pyrimidine ring allows for selective functionalization, enabling chemists to introduce different substituents to tailor the compound's properties for specific applications. The amino group at the 4-position further enhances its utility by providing a site for further derivatization and molecular modifications.When incorporated into synthetic pathways, 5-Bromo-2-methoxypyrimidin-4-amine acts as a crucial starting material for the construction of more complex molecules with desired biological activities. Its role in chemical synthesis extends to the development of new drug candidates, crop protection agents, and other bioactive compounds with potential therapeutic or agricultural applications.