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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-AMINOPYRIMIDINE HYDROCHLORIDE

Nc1ccncn1.Cl Request for Quotation
Chemical Name: 4-AMINOPYRIMIDINE HYDROCHLORIDE
CAS Number: 174500-31-3
Product Number: AG001ZQ0(AGN-PC-0WAJ2C)
Synonyms:
MDL No:
Molecular Formula: C4H6ClN3
Molecular Weight: 131.5635

Identification/Properties

Computed Properties
Molecular Weight:
131.563g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
131.025g/mol
Monoisotopic Mass:
131.025g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
54.9
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 4-Pyrimidinamine hydrochloride (1:1) serves as a versatile building block with diverse applications. This compound plays a crucial role in the construction of various heterocyclic molecules and pharmaceutical intermediates. By participating in key synthetic reactions, such as nucleophilic substitutions and condensations, 4-Pyrimidinamine hydrochloride facilitates the creation of structurally complex compounds with potential biological activities. Its ability to undergo selective transformations under controlled conditions makes it a valuable reagent for the development of novel organic molecules in medicinal chemistry and drug discovery. Additionally, the unique reactivity and functional groups present in 4-Pyrimidinamine hydrochloride offer synthetic chemists a platform for designing customized molecular scaffolds for specific research purposes.