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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)-

2-Amino-5-bromo-4-methoxypyrimidine

COc1nc(N)ncc1Br Request for Quotation
Chemical Name: 2-Amino-5-bromo-4-methoxypyrimidine
CAS Number: 36082-45-8
Product Number: AG003GGI(AGN-PC-07A1HT)
Synonyms:
MDL No: MFCD08460376
Molecular Formula: C5H6BrN3O
Molecular Weight: 204.0246

Identification/Properties

Properties
MP:
125 - 126 °C
BP:
364.794 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
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


2-Amino-5-bromo-4-methoxypyrimidine, a versatile compound in chemical synthesis, plays a crucial role as a building block in the development of various organic molecules. This substance is commonly used as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactivity make it an essential component for the creation of diverse synthetic pathways and functional group manipulations. Additionally, due to its selective functionalization properties, 2-amino-5-bromo-4-methoxypyrimidine serves as a valuable tool for the modification of complex organic molecules, thus enabling the synthesis of novel compounds with enhanced properties and biological activities.