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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)-

1(3H)-Isobenzofuranone, 6-fluoro-

Fc1ccc2c(c1)C(=O)OC2 Request for Quotation
Chemical Name: 1(3H)-Isobenzofuranone, 6-fluoro-
CAS Number: 23932-84-5
Product Number: AG006XRK(AGN-PC-0NH28Z)
Synonyms:
MDL No:
Molecular Formula: C8H5FO2
Molecular Weight: 152.1225

Identification/Properties

Computed Properties
Molecular Weight:
152.124g/mol
XLogP3:
0.9
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-Fluoroisobenzofuran-1(3H)-one, also known as $name$, is a versatile chemical compound that finds widespread application in various chemical synthesis processes. This compound serves as a key building block in the creation of complex organic molecules due to its unique structural properties and reactivity.One of the primary uses of $name$ in chemical synthesis is as a starting material for the preparation of novel pharmaceutical compounds. By utilizing $name$ as a precursor, chemists can introduce specific functional groups and structural motifs into the target molecules, leading to the development of new drugs with improved therapeutic properties.Moreover, 6-Fluoroisobenzofuran-1(3H)-one plays a crucial role in the synthesis of fine chemicals and agrochemicals. Its ability to undergo various chemical transformations, such as nucleophilic substitution and oxidation reactions, allows for the creation of diverse molecular structures that are valuable in the production of high-performance materials and crop protection agents.Additionally, in the field of materials science, $name$ is employed for the fabrication of organic electronic components, including organic light-emitting diodes (OLEDs) and organic photovoltaic devices. Its suitable electron-donating and accepting properties make it a desirable intermediate for constructing functional organic materials with tailored electronic properties.Overall, the application of 6-Fluoroisobenzofuran-1(3H)-one in chemical synthesis extends across various industries, providing chemists with a powerful tool for designing and synthesizing innovative molecules with important industrial and scientific applications.