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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-Indole-2,3-dione, 7-fluoro-, 3-oxime

ON=C1C(=O)Nc2c1cccc2F Request for Quotation
Chemical Name: 1H-Indole-2,3-dione, 7-fluoro-, 3-oxime
CAS Number: 143884-84-8
Product Number: AG001IKG(AGN-PC-0O2QY9)
Synonyms:
MDL No:
Molecular Formula: C8H5FN2O2
Molecular Weight: 180.1359

Identification/Properties

Properties
MP:
248-250
BP:
395.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
180.138g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
180.034g/mol
Monoisotopic Mass:
180.034g/mol
Topological Polar Surface Area:
65.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
214
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Fluoro-3-(hydroxyimino)indolin-2-one is a versatile compound commonly employed in chemical synthesis as a key building block. Specifically, this compound is utilized as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique chemical structure, characterized by the presence of a fluorine atom and a hydroxyimino group, imparts distinctive reactivity and selectivity in synthetic pathways.In organic synthesis, 7-Fluoro-3-(hydroxyimino)indolin-2-one serves as a valuable starting material for the construction of heterocyclic compounds through diverse chemical transformations. Its functional groups allow for site-selective modifications, facilitating the introduction of additional substituents or the formation of new bonds. Furthermore, the presence of the fluorine atom offers the potential for further derivatization through fluorination reactions, enabling access to a broader range of structurally diverse molecules.Moreover, the hydroxyimino functionality of 7-Fluoro-3-(hydroxyimino)indolin-2-one can participate in various types of reactions, such as nucleophilic additions, condensations, and redox processes. This enables the synthesis of complex molecular scaffolds with desired pharmacological or biological activities. Overall, the versatility of this compound makes it a valuable tool for chemists involved in the design and synthesis of novel compounds for various applications.