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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)-

9-([1,1'-Biphenyl]-4-yl)-2-bromo-9H-carbazole

Brc1ccc2c(c1)n(c1ccc(cc1)c1ccccc1)c1c2cccc1 Request for Quotation
Chemical Name: 9-([1,1'-Biphenyl]-4-yl)-2-bromo-9H-carbazole
CAS Number: 1393835-87-4
Product Number: AG001AW4(AGN-PC-0WAMKA)
Synonyms:
MDL No: MFCD27979953
Molecular Formula: C24H16BrN
Molecular Weight: 398.2945

Identification/Properties

Computed Properties
Molecular Weight:
398.3g/mol
XLogP3:
7.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
397.04661g/mol
Monoisotopic Mass:
397.04661g/mol
Topological Polar Surface Area:
4.9Ų
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
465
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 9-([1,1'-Biphenyl]-4-yl)-2-bromo-9H-carbazole plays a crucial role in chemical synthesis as a versatile building block for the development of new materials and organic molecules. Due to its unique structural features, this compound can be utilized in the synthesis of various organic compounds through processes such as Suzuki-Miyaura cross-coupling reactions. By serving as a key intermediate, it enables the efficient construction of complex molecular structures with tailored properties, making it an essential component in the toolbox of synthetic chemists. Its application in chemical synthesis contributes to the advancement of material science and pharmaceutical research by providing access to novel molecules with potential applications in a wide range of fields.