2-(5-bromopyridin-3-yl)oxazole


Chemical Name: 2-(5-bromopyridin-3-yl)oxazole
CAS Number: 342600-96-8
Product Number: AG003EXX(AGN-PC-0WA56V)
Synonyms:
MDL No:
Molecular Formula: C8H5BrN2O
Molecular Weight: 225.0421

Identification/Properties


Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
225.045g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
223.959g/mol
Monoisotopic Mass:
223.959g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
156
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


PNMR/2-5-BROMOPYRIDIN-3-YLOXAZOLE-342600-96-8-hnmr.pdf

Other Analytical Data


POTHER/2-5-BROMOPYRIDIN-3-YLOXAZOLE-342600-96-8-hplc.pdf

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Chemical Structure



2-(5-Bromopyridin-3-yl)oxazole is a versatile compound that finds significant application in chemical synthesis, particularly in the development of novel pharmaceuticals and agrochemicals. This unique molecule acts as a valuable building block in organic synthesis due to its ability to undergo various transformations and participate in diverse chemical reactions.In organic chemistry, 2-(5-Bromopyridin-3-yl)oxazole serves as a key intermediate in the preparation of complex heterocyclic compounds. Its structural features make it a useful starting material for the synthesis of biologically active compounds, such as antiviral agents, antibacterial drugs, and anti-inflammatory medications.Additionally, this compound plays a crucial role in medicinal chemistry research, where it is employed in the design and synthesis of potential drug candidates. By incorporating 2-(5-Bromopyridin-3-yl)oxazole into molecular scaffolds, chemists can explore new chemical space and develop molecules with enhanced pharmacological properties and target selectivity.Moreover, in the field of agricultural chemistry, 2-(5-Bromopyridin-3-yl)oxazole is utilized for the creation of pesticides and herbicides with improved efficacy and environmental safety profiles. By modifying the structure of this compound, researchers can optimize the biological activity of agrochemicals and address challenges related to pest resistance and environmental impact.Overall, the versatile nature of 2-(5-Bromopyridin-3-yl)oxazole makes it a valuable tool in chemical synthesis, offering scientists and researchers the opportunity to explore innovative pathways for the development of therapeutically and agriculturally relevant compounds.