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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)-

7-chloro-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine

Clc1cc(nc2n1ncn2)c1ccccc1 Request for Quotation
Chemical Name: 7-chloro-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine
CAS Number: 28565-43-7
Product Number: AG002VPF(AGN-PC-0LWXI9)
Synonyms:
MDL No:
Molecular Formula: C11H7ClN4
Molecular Weight: 230.6531

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
230.655g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
230.036g/mol
Monoisotopic Mass:
230.036g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
244
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Chloro-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine is a versatile compound commonly employed in chemical synthesis. Its unique structure and reactivity make it an ideal building block for the development of novel pharmaceuticals, agrochemicals, and materials. In organic synthesis, this compound serves as a key intermediate in the preparation of various heterocyclic compounds including triazolopyrimidines, which exhibit diverse biological activities. Additionally, 7-Chloro-5-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine can be utilized in the design and synthesis of molecular probes for biological studies and drug discovery. Its strategic placement of functional groups enables efficient derivatization and modification, allowing for the creation of libraries of analogs for structure-activity relationship studies. This compound's versatility and synthetic utility position it as a valuable tool for the development of new chemical entities with potential applications in both academic research and industrial settings.