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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, 6-chloro-5-fluoro-

O=C1Nc2c(C1=O)cc(c(c2)Cl)F Request for Quotation
Chemical Name: 1H-Indole-2,3-dione, 6-chloro-5-fluoro-
CAS Number: 96202-57-2
Product Number: AG00IJSE(AGN-PC-03FTGO)
Synonyms:
MDL No:
Molecular Formula: C8H3ClFNO2
Molecular Weight: 199.5663

Identification/Properties

Computed Properties
Molecular Weight:
199.565g/mol
XLogP3:
1.6
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


5-Fluoro-6-chloroisatin is a versatile chemical compound that finds wide 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 structure and reactivity. In the realm of chemical synthesis, 5-Fluoro-6-chloroisatin acts as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.One prominent application of 5-Fluoro-6-chloroisatin in chemical synthesis is its role as a precursor in the preparation of heterocyclic compounds. By undergoing a series of well-defined chemical reactions, 5-Fluoro-6-chloroisatin can be transformed into structurally diverse molecules with enhanced biological activities or specific functionalities. This ability makes it a crucial component in the synthesis of novel drug candidates, pesticides, and other fine chemicals.Furthermore, 5-Fluoro-6-chloroisatin can participate in various cross-coupling reactions and functional group transformations, enabling chemists to introduce specific functional groups at precise positions in a target molecule. This level of control is essential in designing molecules with desired properties, such as improved potency, selectivity, or solubility. The versatility of 5-Fluoro-6-chloroisatin allows chemists to access a wide range of chemical space and explore new avenues for molecular design.Overall, the strategic use of 5-Fluoro-6-chloroisatin in chemical synthesis empowers researchers to streamline the synthesis of complex molecules, accelerate the discovery of novel compounds, and advance the fields of pharmaceuticals, agrochemicals, and materials science. Its versatility and reactivity make it a valuable tool for synthetic chemists seeking to push the boundaries of molecular design and synthesis.