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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)-

Anthracene, 9-bromo-10-phenyl-

Brc1c2ccccc2c(c2c1cccc2)c1ccccc1 Request for Quotation
Chemical Name: Anthracene, 9-bromo-10-phenyl-
CAS Number: 23674-20-6
Product Number: AG002O41(AGN-PC-0L6BAQ)
Synonyms:
MDL No:
Molecular Formula: C20H13Br
Molecular Weight: 333.2212

Identification/Properties

Computed Properties
Molecular Weight:
333.228g/mol
XLogP3:
6.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
332.02g/mol
Monoisotopic Mass:
332.02g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
322
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#:
-
Hazard Statements:
H302-H315-H317-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


9-Bromo-10-phenylanthracene is a versatile compound commonly used in chemical synthesis. Its unique structure allows for various applications in the field of organic chemistry. One of the key uses of this compound is as a building block in the synthesis of complex organic molecules and materials.Due to its bromine functional group, 9-Bromo-10-phenylanthracene can participate in a wide range of reactions such as Suzuki couplings, Heck reactions, and Buchwald-Hartwig cross-coupling reactions. These reactions enable chemists to introduce the 9-bromo-10-phenylanthracene moiety into more intricate structures, thereby expanding the scope of potential compounds that can be synthesized.Additionally, 9-Bromo-10-phenylanthracene serves as a valuable intermediate in the production of functionalized anthracene derivatives, which are commonly employed in the development of organic semiconductors, dyes, and pharmaceuticals. Its ability to undergo various transformations makes it a crucial component in the toolbox of synthetic chemists seeking to create novel molecules with tailored properties.Overall, 9-Bromo-10-phenylanthracene plays a crucial role in advancing chemical synthesis by providing a platform for the construction of complex organic molecules with enhanced functionality and diverse applications.