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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-methoxypyrimidin-4-yl)methanamine

COc1nccc(n1)CN Request for Quotation
Chemical Name: (2-methoxypyrimidin-4-yl)methanamine
CAS Number: 944901-04-6
Product Number: AG00H6CW(AGN-PC-0ALQ7W)
Synonyms:
MDL No:
Molecular Formula: C6H9N3O
Molecular Weight: 139.1552

Identification/Properties

Properties
BP:
280.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
139.158g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
139.075g/mol
Monoisotopic Mass:
139.075g/mol
Topological Polar Surface Area:
61A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
99
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methoxypyrimidin-4-yl)methanamine is a versatile compound commonly used in chemical synthesis due to its functional groups and reactivity. This compound is frequently employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and various organic compounds. Its amine group allows for facile modification through common synthetic reactions, such as acylation, alkylation, and cross-coupling reactions. Additionally, the pyrimidine scaffold serves as a valuable building block for the construction of more complex molecules. In the field of medicinal chemistry, (2-Methoxypyrimidin-4-yl)methanamine plays a crucial role in the development of novel drug candidates targeting a wide range of biological pathways. Its unique structure and reactivity make it a valuable tool for chemists seeking to design and synthesize new compounds with diverse functions and properties.