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  2. 8-bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine

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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)-

8-bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine

Cc1cc(Br)c2n(c1)ncn2 Request for Quotation
Chemical Name: 8-bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine
CAS Number: 957062-94-1
Product Number: AG00IJDO(AGN-PC-0589TF)
Synonyms:
MDL No:
Molecular Formula: C7H6BrN3
Molecular Weight: 212.0466

Identification/Properties

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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine is a versatile compound commonly employed in chemical synthesis for its unique properties and reactivity. This heterocyclic molecule serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 8-Bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine plays a crucial role as a key intermediate in the preparation of novel drug candidates and bioactive molecules. Its structural features make it an ideal precursor for the introduction of functional groups and modifications, enabling chemists to fine-tune the properties of the final product. Furthermore, the presence of the bromine substituent in 8-Bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine offers a handle for further derivatization through various chemical transformations such as nucleophilic substitution, palladium-catalyzed cross-coupling reactions, or metal-catalyzed coupling reactions. This flexibility makes it a valuable tool for designing and synthesizing complex organic molecules with specific biological or physicochemical properties.Overall, the strategic use of 8-Bromo-6-methyl-[1,2,4]triazolo[1,5-a]pyridine in chemical synthesis highlights its significance as a versatile building block for the creation of diverse compounds with potential applications in the fields of pharmaceuticals, materials science, and agrochemicals.