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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)-

4-bromo-6-fluoro-1H-indole

Fc1cc(Br)c2c(c1)[nH]cc2 Request for Quotation
Chemical Name: 4-bromo-6-fluoro-1H-indole
CAS Number: 885520-70-7
Product Number: AG00GWQU(AGN-PC-04Q58X)
Synonyms:
MDL No: MFCD08272203
Molecular Formula: C8H5BrFN
Molecular Weight: 214.0344

Identification/Properties

Computed Properties
Molecular Weight:
214.037g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
212.959g/mol
Monoisotopic Mass:
212.959g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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


4-Bromo-6-fluoro-1H-indole is a versatile chemical compound with significant applications in chemical synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structural properties make it a crucial intermediate in the synthesis of diverse organic compounds.In organic synthesis, 4-Bromo-6-fluoro-1H-indole is commonly used as a key reactant in the creation of complex molecules with desirable properties. Its presence allows for the introduction of specific functional groups and structural motifs that are essential for the development of new drugs, crop protection agents, and advanced materials.By incorporating 4-Bromo-6-fluoro-1H-indole into synthetic pathways, chemists can access a wide range of derivatives with tailored chemical properties. The versatility of this compound enables the creation of molecules with diverse biological activities, making it a valuable tool in medicinal chemistry and drug discovery efforts.Furthermore, the presence of both bromine and fluorine substituents in 4-Bromo-6-fluoro-1H-indole adds additional versatility to its synthetic utility. These functional groups can undergo various transformations, such as cross-coupling reactions and nucleophilic substitutions, leading to the generation of structurally complex and biologically relevant compounds.Overall, 4-Bromo-6-fluoro-1H-indole plays a crucial role in chemical synthesis by serving as a strategic building block for the construction of diverse organic molecules with applications in pharmaceutical, agricultural, and materials science industries.