1H-Indole, 2-(3-bromophenyl)-|93716-78-0,AngeneChemical

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1H-Indole, 2-(3-bromophenyl)-

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Chemical Name:	1H-Indole, 2-(3-bromophenyl)-
CAS Number:	93716-78-0
Product Number:	AG00IHRK(AGN-PC-00ONKA)
Synonyms:
MDL No:
Molecular Formula:	C14H10BrN
Molecular Weight:	272.1399

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Identification/Properties

Computed Properties

Molecular Weight:

272.145g/mol

XLogP3:

4.4

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

271g/mol

Monoisotopic Mass:

271g/mol

Topological Polar Surface Area:

15.8A^2

Heavy Atom Count:

Formal Charge:

Complexity:

243

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure

2-(3-Bromophenyl)-1H-indole, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique structural properties and reactivity. This compound is commonly employed as a key building block in the preparation of various pharmaceuticals, agrochemicals, and organic materials.In organic synthesis, $name$ serves as a valuable starting material for the synthesis of complex molecules with indole moieties. Its bromine functional group allows for further derivatization through various chemical transformations, such as nucleophilic substitution reactions, Suzuki coupling, and palladium-catalyzed cross-coupling reactions.Additionally, the presence of the indole ring in 2-(3-Bromophenyl)-1H-indole imparts aromaticity and electron-rich properties, making it a versatile substrate for the construction of bioactive compounds and molecular scaffolds. Its significance extends to the development of potential drug candidates targeting various therapeutic areas, including cancer, neurological disorders, and infectious diseases.Furthermore, the strategic incorporation of 2-(3-Bromophenyl)-1H-indole in chemical synthesis enables chemists to access diverse structural motifs and functional groups, facilitating the exploration of new synthetic pathways and molecular designs. Its utility in medicinal chemistry, material science, and chemical biology underscores its importance as a valuable tool for innovation and discovery in the field of organic chemistry.