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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)-

Pentacene, 6,13-diphenyl-

c1ccc(cc1)c1c2cc3ccccc3cc2c(c2c1cc1ccccc1c2)c1ccccc1 Request for Quotation
Chemical Name: Pentacene, 6,13-diphenyl-
CAS Number: 76727-11-2
Product Number: AG008PG4(AGN-PC-0048P5)
Synonyms:
MDL No:
Molecular Formula: C34H22
Molecular Weight: 430.5385

Identification/Properties

Computed Properties
Molecular Weight:
430.55g/mol
XLogP3:
10.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
430.172g/mol
Monoisotopic Mass:
430.172g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
570
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,13-Diphenylpentacene is a valuable compound in chemical synthesis, particularly in the field of organic electronics and materials science. It serves as a key building block for the production of organic semiconductors due to its unique π-conjugated structure. This compound is widely utilized in the development of organic field-effect transistors (OFETs), organic photovoltaic (OPV) devices, and organic light-emitting diodes (OLEDs).In chemical synthesis, 6,13-Diphenylpentacene is commonly employed as a precursor in the preparation of more complex organic molecules with enhanced electronic properties. By incorporating this versatile compound into various molecular structures, researchers can tailor the optical and electronic properties of the resulting materials for specific applications. Additionally, the ability of 6,13-Diphenylpentacene to undergo various functionalization reactions enables the introduction of different substituents or side chains, further expanding its utility in the synthesis of advanced organic materials.Overall, the use of 6,13-Diphenylpentacene in chemical synthesis offers researchers a versatile and powerful tool for designing and fabricating organic materials with tailored electronic properties, making it a valuable component in the development of next-generation electronics and optoelectronic devices.