2-bromo-9-phenylcarbazole|94994-62-4,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

2-bromo-9-phenylcarbazole

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Chemical Name:	2-bromo-9-phenylcarbazole
CAS Number:	94994-62-4
Product Number:	AG00IIOE(AGN-PC-0H6HIE)
Synonyms:
MDL No:
Molecular Formula:	C18H12BrN
Molecular Weight:	322.1986

Identification/Properties
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Identification/Properties

Computed Properties

Molecular Weight:

322.205g/mol

XLogP3:

5.7

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

321.015g/mol

Monoisotopic Mass:

321.015g/mol

Topological Polar Surface Area:

4.9A^2

Heavy Atom Count:

Formal Charge:

Complexity:

338

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-Bromo-9-phenyl-9H-carbazole, a versatile compound widely used in chemical synthesis, serves as a key building block in the creation of various organic molecules. With its unique structure and reactivity, this chemical plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials. Specifically, 2-Bromo-9-phenyl-9H-carbazole is commonly utilized in cross-coupling reactions to form C-C bonds and as a precursor in the synthesis of complex heterocyclic compounds. Its strategic incorporation enables chemists to access a diverse array of molecular structures with tailored properties, making it a valuable tool for modern organic synthesis strategies.