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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]pyridine, 6-bromo-5-methyl-

Brc1ccc2n(c1C)ncn2 Request for Quotation
Chemical Name: [1,2,4]Triazolo[1,5-a]pyridine, 6-bromo-5-methyl-
CAS Number: 746668-59-7
Product Number: AG005IHL(AGN-PC-00D06N)
Synonyms:
MDL No:
Molecular Formula: C7H6BrN3
Molecular Weight: 212.0466

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
212.05g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
210.975g/mol
Monoisotopic Mass:
210.975g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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


6-Bromo-5-methyl[1,2,4]triazolo[1,5-a]pyridine is a versatile chemical compound that finds widespread application in organic synthesis. This specific compound serves as a valuable building block in the creation of various biologically active molecules and pharmaceutical compounds. Its unique structure enables it to participate in diverse chemical reactions, making it an essential component in the synthesis of complex organic molecules. From facilitating ring formation to serving as a scaffold for further derivatization, 6-Bromo-5-methyl[1,2,4]triazolo[1,5-a]pyridine plays a crucial role in the construction of novel chemical entities with potential applications in drug discovery and material science industries.