1. Home
  2. [1,2,4]Triazolo[1,5-a]pyridine, 6-bromo-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-

Brc1ccc2n(c1)ncn2 Request for Quotation
Chemical Name: [1,2,4]Triazolo[1,5-a]pyridine, 6-bromo-
CAS Number: 356560-80-0
Product Number: AG00BYH9(AGN-PC-00AN52)
Synonyms:
MDL No: MFCD08689534
Molecular Formula: C6H4BrN3
Molecular Weight: 198.0201

Identification/Properties

Computed Properties
Molecular Weight:
198.023g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
196.959g/mol
Monoisotopic Mass:
196.959g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
130
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

Request for Quotation

Customer Feedback

Chemical Structure


6-Bromo-[1,2,4]triazolo[1,5-a]pyridine is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the synthesis of various compounds, particularly in the pharmaceutical and agrochemical industries. This compound is often utilized as a key intermediate in the synthesis of biologically active molecules, such as pharmaceutical drugs, herbicides, and fungicides. Its ability to undergo various chemical reactions, such as nucleophilic substitutions and cross-coupling reactions, allows for the efficient construction of complex molecular structures.In medicinal chemistry, 6-Bromo-[1,2,4]triazolo[1,5-a]pyridine serves as a core scaffold for the development of novel drug candidates targeting a wide range of therapeutic areas. Its presence in the molecular structure can impart desirable pharmacological properties or enhance the biological activity of the final compound.Additionally, this compound is a valuable tool in the exploration of chemical reactions and mechanisms in organic synthesis. Its controlled reactivity and compatibility with a variety of functional groups make it a versatile and reliable building block for the construction of diverse molecular architectures.Overall, the application of 6-Bromo-[1,2,4]triazolo[1,5-a]pyridine in chemical synthesis enables the rapid and efficient preparation of valuable compounds with potential applications in drug discovery, agricultural chemistry, and material science.