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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)-

3(2H)-Benzofuranone, 6-fluoro-

Fc1ccc2c(c1)OCC2=O Request for Quotation
Chemical Name: 3(2H)-Benzofuranone, 6-fluoro-
CAS Number: 351528-80-8
Product Number: AG003N7U(AGN-PC-01UUCD)
Synonyms:
MDL No: MFCD09743984
Molecular Formula: C8H5FO2
Molecular Weight: 152.1225

Identification/Properties

Properties
BP:
261.7±40.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Fluorobenzofuran-3(2H)-one is a versatile compound that finds wide application in chemical synthesis. Its unique structure containing a fluorine atom attached to a benzofuran ring imparts specific properties that make it valuable in various organic reactions. This compound is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. With its fluorine substituent, 6-Fluorobenzofuran-3(2H)-one can participate in diverse reactions such as nucleophilic aromatic substitution, metal-catalyzed cross-coupling reactions, and as a directing group in C-H functionalization. Its utility in the production of complex molecules makes it a crucial intermediate in the synthesis of biologically active compounds and advanced materials.