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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)-

4-fluoro-1-benzofuran-3-one

O=C1COc2c1c(F)ccc2 Request for Quotation
Chemical Name: 4-fluoro-1-benzofuran-3-one
CAS Number: 911826-36-3
Product Number: AG00IGIX(AGN-PC-07AUXV)
Synonyms:
MDL No:
Molecular Formula: C8H5FO2
Molecular Weight: 152.1225

Identification/Properties

Computed Properties
Molecular Weight:
152.124g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
152.027g/mol
Monoisotopic Mass:
152.027g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
181
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

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Chemical Structure


4-Fluorobenzofuran-3(2H)-one is a versatile compound commonly utilized in chemical synthesis for various applications. With its unique structure and properties, this molecule serves as a valuable building block in organic synthesis, enabling the creation of intricate and specialized compounds. In particular, 4-Fluorobenzofuran-3(2H)-one is often employed in the development of pharmaceuticals, agrochemicals, and materials science. Its involvement in these fields highlights its significance in driving innovation and advancements in the chemical industry.Furthermore, the reactivity of 4-Fluorobenzofuran-3(2H)-one allows for efficient functionalization, making it a pivotal component in the synthesis of complex molecules with specific properties. Through strategic manipulation and derivatization, chemists can tailor the structure of the compound to suit the desired application, showcasing the adaptability and utility of this molecule in various chemical processes. Overall, the inclusion of 4-Fluorobenzofuran-3(2H)-one in chemical synthesis underscores its importance as a key ingredient for the development of novel compounds with diverse functionalities.