3H-1,2,3-Triazolo[4,5-b]pyridine,6-bromo-


Chemical Name: 3H-1,2,3-Triazolo[4,5-b]pyridine,6-bromo-
CAS Number: 92276-38-5
Product Number: AG003N46(AGN-PC-0VYZL7)
Synonyms:
MDL No:
Molecular Formula: C5H3BrN4
Molecular Weight: 199.0081

Identification/Properties


Properties
MP:
209 °C
BP:
272.9 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
199.011g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
197.954g/mol
Monoisotopic Mass:
197.954g/mol
Topological Polar Surface Area:
54.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
131
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



6-Bromo-3H-[1,2,3]triazolo[4,5-b]pyridine is a highly versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the preparation of various organic molecules. In particular, this compound is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.One of the key applications of 6-Bromo-3H-[1,2,3]triazolo[4,5-b]pyridine is as a precursor in the preparation of heterocyclic compounds. Its 3H-[1,2,3]triazolo[4,5-b]pyridine scaffold serves as a valuable template for the construction of complex molecules with diverse biological activities. By functionalizing the bromine atom, chemists can introduce different substituents to tailor the properties of the final product.Furthermore, 6-Bromo-3H-[1,2,3]triazolo[4,5-b]pyridine can participate in various types of chemical reactions, including coupling reactions, nucleophilic substitutions, and cycloadditions. These reactivity profiles make it a versatile intermediate in the synthesis of target molecules with strategic bond formations.Overall, the strategic use of 6-Bromo-3H-[1,2,3]triazolo[4,5-b]pyridine in chemical synthesis enables the efficient construction of complex organic molecules with tailored properties for a range of applications in the fields of pharmaceuticals, agrochemicals, and materials science.