1,2-Benzisoxazol-3(2H)-one, 5-fluoro-


Chemical Name: 1,2-Benzisoxazol-3(2H)-one, 5-fluoro-
CAS Number: 99822-23-8
Product Number: AG003W7N(AGN-PC-0052KT)
Synonyms:
MDL No:
Molecular Formula: C7H4FNO2
Molecular Weight: 153.1106

Identification/Properties


Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
153.112g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
153.023g/mol
Monoisotopic Mass:
153.023g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
185
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-Fluorobenzo[d]isoxazol-3(2H)-one, also known as $name$, is a versatile chemical compound frequently employed in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and functional groups make it an essential tool in the field of organic chemistry.One significant application of 5-Fluorobenzo[d]isoxazol-3(2H)-one lies in its use as a starting material for the synthesis of heterocyclic compounds. By utilizing the reactivity of the fluorine atom and the isoxazole ring, chemists can introduce diverse functional groups onto the molecule, facilitating the construction of complex structures with specific biological or physical properties.Furthermore, 5-Fluorobenzo[d]isoxazol-3(2H)-one is often employed in the development of novel drug candidates due to its potential pharmacological activities. By incorporating this compound into drug design, researchers can explore new avenues for therapeutic interventions, targeting various diseases and medical conditions.In summary, 5-Fluorobenzo[d]isoxazol-3(2H)-one plays a crucial role in chemical synthesis by enabling the construction of intricate molecules with diverse applications in the pharmaceutical and materials science industries. Its versatility and reactivity make it a valuable tool for scientists seeking to innovate and advance their research in organic chemistry.