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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, 3-bromo-1-(phenylsulfonyl)-

Brc1cn(c2c1cccc2)S(=O)(=O)c1ccccc1 Request for Quotation
Chemical Name: 1H-Indole, 3-bromo-1-(phenylsulfonyl)-
CAS Number: 99655-68-2
Product Number: AG003IZ9(AGN-PC-0KKXDB)
Synonyms:
MDL No:
Molecular Formula: C14H10BrNO2S
Molecular Weight: 336.2037

Identification/Properties

Properties
MP:
122-126 °C(lit.)
BP:
498 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
336.203g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
334.962g/mol
Monoisotopic Mass:
334.962g/mol
Topological Polar Surface Area:
47.4A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
414
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


3-Bromo-1-(phenylsulfonyl)-1H-indole is a versatile compound that serves as a valuable building block in chemical synthesis. This unique molecule is widely used as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. One of the primary applications of 3-Bromo-1-(phenylsulfonyl)-1H-indole lies in its utility as a potent electrophilic reagent in organic reactions. Its bromo functionality allows for selective cross-coupling reactions with different nucleophiles, enabling the efficient construction of complex molecular structures. Additionally, the presence of the sulfonyl group enhances the reactivity of the molecule, facilitating diverse transformations in synthetic pathways.Furthermore, 3-Bromo-1-(phenylsulfonyl)-1H-indole can be employed in the synthesis of biologically active compounds such as antibacterial agents, anti-inflammatory drugs, and anticancer therapies. Its indole core provides a critical structural motif found in many bioactive molecules, making it a valuable scaffold for medicinal chemistry research.Overall, the strategic incorporation of 3-Bromo-1-(phenylsulfonyl)-1H-indole in chemical synthesis offers a powerful tool for the efficient and selective construction of valuable compounds with a wide range of potential applications.