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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)-

Benzonitrile, 4,4'-carbonylbis-

N#Cc1ccc(cc1)C(=O)c1ccc(cc1)C#N Request for Quotation
Chemical Name: Benzonitrile, 4,4'-carbonylbis-
CAS Number: 32446-66-5
Product Number: AG0033UO(AGN-PC-0N8BHY)
Synonyms:
MDL No:
Molecular Formula: C15H8N2O
Molecular Weight: 232.2368

Identification/Properties

Properties
MP:
>151°C (dec.)
BP:
457.782°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
232.242g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
232.064g/mol
Monoisotopic Mass:
232.064g/mol
Topological Polar Surface Area:
64.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
357
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


4,4'-Dicyanobenzophenone is a versatile compound widely used in chemical synthesis as a powerful building block for the creation of various organic molecules. Its unique structure and reactivity make it an essential reagent in the production of pharmaceuticals, polymers, and other fine chemicals. In particular, 4,4'-Dicyanobenzophenone is commonly employed in the synthesis of dyes, pigments, and fluorescent compounds due to its ability to introduce cyanide groups into aromatic systems. Additionally, its high electrophilicity makes it a valuable tool in the formation of carbon-carbon and carbon-heteroatom bonds, enabling the construction of complex molecular architectures with precision and efficiency. In summary, the application of 4,4'-Dicyanobenzophenone in chemical synthesis showcases its utility as a strategic intermediate for the development of diverse organic compounds with tailored properties and functions.