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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)-

6-chloro-7-fluoro-1H-indole-2,3-dione

O=C1C(=O)Nc2c1ccc(c2F)Cl Request for Quotation
Chemical Name: 6-chloro-7-fluoro-1H-indole-2,3-dione
CAS Number: 942493-23-4
Product Number: AG00GUYQ(AGN-PC-05FQJA)
Synonyms:
MDL No:
Molecular Formula: C8H3ClFNO2
Molecular Weight: 199.5663

Identification/Properties

Computed Properties
Molecular Weight:
199.565g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
198.984g/mol
Monoisotopic Mass:
198.984g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
271
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


6-Chloro-7-fluoroindoline-2,3-dione is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and materials due to its ability to undergo diverse chemical reactions.One of the key applications of 6-Chloro-7-fluoroindoline-2,3-dione in chemical synthesis is its role as a key intermediate in the synthesis of heterocyclic compounds. By utilizing this compound as a starting material, chemists can efficiently access a range of structurally diverse molecules with significant biological and pharmacological activities. Additionally, the presence of both chlorine and fluorine functional groups in this compound enhances its reactivity and enables the introduction of specific substituents in the target molecules.Furthermore, 6-Chloro-7-fluoroindoline-2,3-dione is often employed in transition-metal-catalyzed reactions to facilitate complex bond formations. Its unique structure allows for precise control over regioselectivity and stereoselectivity in various synthetic transformations, making it a valuable tool in the creation of intricate organic molecules.In summary, the application of 6-Chloro-7-fluoroindoline-2,3-dione in chemical synthesis offers chemists a strategic and efficient route to access diverse heterocyclic compounds with tailored properties and functionalities.