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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)-

3-bromo-9-naphthalen-2-ylcarbazole

Brc1ccc2c(c1)c1ccccc1n2c1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: 3-bromo-9-naphthalen-2-ylcarbazole
CAS Number: 934545-80-9
Product Number: AG00H17N(AGN-PC-0HVKSF)
Synonyms:
MDL No:
Molecular Formula: C22H14BrN
Molecular Weight: 372.2573

Identification/Properties

Computed Properties
Molecular Weight:
372.265g/mol
XLogP3:
6.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
371.031g/mol
Monoisotopic Mass:
371.031g/mol
Topological Polar Surface Area:
4.9A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
451
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:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-9-(naphthalen-2-yl)-9H-carbazole, also known as $name$, is a highly versatile compound that finds extensive applications in organic chemical synthesis. One of its key uses lies in its utility as a valuable building block for the synthesis of various functional organic materials. In chemical synthesis, $name$ serves as a crucial intermediate in the preparation of advanced materials such as organic semiconductors, dyes, and pharmaceutical compounds. Its unique structure and reactivity facilitate the efficient construction of complex molecular structures with tailored properties. Furthermore, the presence of the bromine moiety in 3-Bromo-9-(naphthalen-2-yl)-9H-carbazole enables diverse functionalization reactions, allowing for the incorporation of additional substituents or modifications to fine-tune the properties of the final products. This versatility makes it a valuable tool for chemists and researchers seeking to design and develop novel compounds for various applications.$name$'s role in chemical synthesis extends beyond its function as a building block, as its incorporation into molecular frameworks can impart specific electronic and optical properties desirable for applications in fields such as optoelectronics, materials science, and medicinal chemistry. Its strategic placement within a molecular structure can influence factors such as energy levels, charge transport, and photophysical properties, making it an indispensable component in the development of advanced functional materials.Overall, the significance of 3-Bromo-9-(naphthalen-2-yl)-9H-carbazole in chemical synthesis lies in its ability to enable the construction of complex organic molecules with tailored functionalities, offering a pathway for the creation of innovative materials with applications across multiple scientific disciplines.