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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)-

4-Pyrimidinamine, 2-methyl-6-(1-methylethyl)-

Nc1cc(nc(n1)C)C(C)C Request for Quotation
Chemical Name: 4-Pyrimidinamine, 2-methyl-6-(1-methylethyl)-
CAS Number: 95206-97-6
Product Number: AG003KQG(AGN-PC-00MAHT)
Synonyms:
MDL No: MFCD09909804
Molecular Formula: C8H13N3
Molecular Weight: 151.2089

Identification/Properties

Properties
BP:
256.6±20.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
151.213g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
151.111g/mol
Monoisotopic Mass:
151.111g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
125
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-Amino-6-isopropyl-2-methylpyrimidine is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its structural characteristics, 4-Amino-6-isopropyl-2-methylpyrimidine can undergo various chemical reactions such as alkylation, acylation, and condensation, making it an essential intermediate in the synthesis of complex organic molecules. Additionally, its presence in the molecular structure can enhance the biological activity of the final products, making it a valuable component in drug discovery and development processes.