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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)-

[1,2,4]Triazolo[1,5-a]pyrimidin-2-amine

Nc1nn2c(n1)nccc2 Request for Quotation
Chemical Name: [1,2,4]Triazolo[1,5-a]pyrimidin-2-amine
CAS Number: 13223-53-5
Product Number: AG0010FB(AGN-PC-0KPZK6)
Synonyms:
MDL No:
Molecular Formula: C5H5N5
Molecular Weight: 135.1267

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
135.13g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
135.054g/mol
Monoisotopic Mass:
135.054g/mol
Topological Polar Surface Area:
69.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
127
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

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Chemical Structure


[1,2,4]Triazolo[1,5-a]pyrimidin-2-amine is a versatile compound widely utilized in chemical synthesis as a building block for the creation of various pharmaceuticals, agrochemicals, and functional materials. This molecule acts as a key intermediate in the synthesis of biologically active compounds due to its unique structure and reactivity.In chemical synthesis, [1,2,4]Triazolo[1,5-a]pyrimidin-2-amine is often employed as a core scaffold for the construction of diverse chemical entities with potential pharmacological properties. Its ability to undergo various transformations, such as functional group modifications and heterocyclic ring formations, makes it an essential component in the development of novel drugs and bioactive molecules.Additionally, researchers utilize [1,2,4]Triazolo[1,5-a]pyrimidin-2-amine in the creation of molecular probes and diagnostic agents for biological studies. Its compatibility with different synthetic methodologies enables the incorporation of specific functionalities that enhance the target interactions and biological activities of the final compounds.Overall, the application of [1,2,4]Triazolo[1,5-a]pyrimidin-2-amine in chemical synthesis plays a crucial role in the discovery and optimization of new molecules with potential therapeutic benefits and biological activities.