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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-(4-broMophenyl)-10-(naphthalen-2-yl)anthracene

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Chemical Name: 9-(4-broMophenyl)-10-(naphthalen-2-yl)anthracene
CAS Number: 936854-62-5
Product Number: AG00H2R5(AGN-PC-0WAKH8)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
459.386g/mol
XLogP3:
9.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
458.067g/mol
Monoisotopic Mass:
458.067g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
567
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


9-(4-Bromophenyl)-10-(naphthalen-2-yl)anthracene is a versatile compound widely used in chemical synthesis as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. This compound plays a crucial role in the development of various organic reactions, including Suzuki coupling, Sonogashira coupling, and Heck reaction. Its unique structure allows for the formation of complex organic molecules with high selectivity and efficiency. Additionally, its aromatic nature and functional groups make it an ideal building block for the synthesis of novel compounds with diverse applications in the field of organic chemistry.