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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)-

7-amino-5-fluoro-1,3-dihydroindol-2-one

O=C1Cc2c(N1)c(N)cc(c2)F Request for Quotation
Chemical Name: 7-amino-5-fluoro-1,3-dihydroindol-2-one
CAS Number: 945381-62-4
Product Number: AG00H60I(AGN-PC-0CV5P4)
Synonyms:
MDL No:
Molecular Formula: C8H7FN2O
Molecular Weight: 166.1524

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
166.155g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
166.054g/mol
Monoisotopic Mass:
166.054g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
209
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


7-Amino-5-fluoroindolin-2-one is a versatile compound commonly used in chemical synthesis due to its unique structural properties and reactivity. It serves as a valuable building block in the production of various pharmaceuticals, agricultural chemicals, and functional materials.In chemical synthesis, 7-Amino-5-fluoroindolin-2-one can be utilized as a key intermediate in the preparation of indole derivatives, which are important structural motifs found in many biologically active compounds. Its amino and fluorine functionalities make it a valuable precursor for introducing these groups into target molecules, allowing for the fine-tuning of their physical and chemical properties.Furthermore, the presence of an amino group on the indole ring provides opportunities for further functionalization through various synthetic methods. This enables chemists to modify the compound to tailor its properties for specific applications in drug discovery, material science, and other fields.Overall, the versatility and reactivity of 7-Amino-5-fluoroindolin-2-one make it an essential building block in chemical synthesis, offering a wide range of possibilities for creating novel compounds with potential pharmaceutical, agricultural, and materials applications.