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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)-

1H-Isoindole-1,3(2H)-dione, 5-fluoro-

Fc1ccc2c(c1)C(=O)NC2=O Request for Quotation
Chemical Name: 1H-Isoindole-1,3(2H)-dione, 5-fluoro-
CAS Number: 94514-21-3
Product Number: AG00JNWJ(AGN-PC-0NCH26)
Synonyms:
MDL No:
Molecular Formula: C8H4FNO2
Molecular Weight: 165.1213

Identification/Properties

Computed Properties
Molecular Weight:
165.123g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
165.023g/mol
Monoisotopic Mass:
165.023g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
241
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


5-Fluoroisoindoline-1,3-dione is a versatile compound that finds wide application in chemical synthesis. This compound serves as a key building block in the preparation of various organic molecules due to its unique reactivity and structural properties. One prominent use of 5-Fluoroisoindoline-1,3-dione is its function as a precursor in the synthesis of pharmaceutical intermediates. It is commonly employed in the pharmaceutical industry for the creation of important drug molecules through a series of synthetic transformations. Additionally, this compound is utilized in the development of advanced materials and fine chemicals, where its distinct chemical reactivity plays a crucial role in creating complex molecular structures. In organic synthesis, 5-Fluoroisoindoline-1,3-dione acts as a valuable starting material for the construction of diverse molecular frameworks with strategic bond formations. Its versatility and utility make it a valuable tool for chemists engaged in the design and preparation of novel compounds with diverse applications.