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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-Pyrimidinamine, 4-(4-methoxyphenyl)-

COc1ccc(cc1)c1ccnc(n1)N Request for Quotation
Chemical Name: 2-Pyrimidinamine, 4-(4-methoxyphenyl)-
CAS Number: 99844-02-7
Product Number: AG003W19(AGN-PC-0KK71Q)
Synonyms:
MDL No:
Molecular Formula: C11H11N3O
Molecular Weight: 201.2245

Identification/Properties

Properties
BP:
434.0±47.0°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
201.229g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
201.09g/mol
Monoisotopic Mass:
201.09g/mol
Topological Polar Surface Area:
61A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
192
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-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


4-(4-Methoxyphenyl)pyrimidin-2-amine, also known as $name$, is a versatile compound that finds wide application in chemical synthesis. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its structural features provide a platform for the incorporation of different functional groups, enabling the creation of diverse molecular structures with specific properties.One of the primary applications of 4-(4-Methoxyphenyl)pyrimidin-2-amine is in the design and synthesis of bioactive molecules. By modifying the amine and pyrimidine moieties, chemists can fine-tune the pharmacological properties of the resulting compounds, making them potential candidates for drug discovery and development. Additionally, this compound can be utilized in the preparation of molecular probes and fluorescent dyes for use in biological studies and imaging techniques.In the field of materials science, 4-(4-Methoxyphenyl)pyrimidin-2-amine plays an essential role in the construction of functional materials with specific electronic or optical properties. Through rational design and manipulation of its chemical structure, researchers can tailor the compound for applications in organic electronics, light-emitting diodes, sensors, and other advanced materials.Overall, the versatility and reactivity of 4-(4-Methoxyphenyl)pyrimidin-2-amine make it a valuable tool in chemical synthesis, offering endless possibilities for the creation of novel compounds with diverse applications in various scientific disciplines.