5-(3-bromophenyl)-1,3-oxazole


Chemical Name: 5-(3-bromophenyl)-1,3-oxazole
CAS Number: 243455-57-4
Product Number: AG003M4G(AGN-PC-0KL7MH)
Synonyms:
MDL No: MFCD05668970
Molecular Formula: C9H6BrNO
Molecular Weight: 224.0540

Identification/Properties


Properties
MP:
57-61 °C
BP:
303.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
224.057g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
222.963g/mol
Monoisotopic Mass:
222.963g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
154
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-(3-Bromophenyl)oxazole, commonly referred to as $name$, is a versatile compound that finds wide application in chemical synthesis. In organic chemistry, it serves as a key building block for the construction of various complex molecules. Due to its unique structure, $name$ is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials. Its bromine substituent provides a valuable handle for further functionalization, allowing chemists to tailor its properties for specific applications.In the field of medicinal chemistry, 5-(3-Bromophenyl)oxazole has been utilized in the design and synthesis of potential drug candidates. Its structural motif offers opportunities for optimizing biological activity and enhancing drug-like properties. Researchers have explored the incorporation of $name$ into drug molecules targeting various therapeutic areas, harnessing its versatile reactivity to modulate pharmacological profiles.Moreover, in the realm of materials science, 5-(3-Bromophenyl)oxazole has demonstrated utility in the preparation of functional materials with tailored properties. By incorporating $name$ into polymer chains or as a functional group in organic frameworks, chemists can control the physical and chemical attributes of the resulting materials. This has led to the development of novel materials for diverse applications, ranging from electronics to coatings.Overall, the strategic incorporation of 5-(3-Bromophenyl)oxazole in chemical synthesis enables the creation of molecules and materials with enhanced functionality and specificity. Its versatility and reactivity make it a valuable tool for synthetic chemists seeking to design advanced compounds for various industrial and research purposes.