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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)-

Benzenamine, 4,4'-(9H-fluoren-9-ylidene)bis-

Nc1ccc(cc1)C1(c2ccc(cc2)N)c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Benzenamine, 4,4'-(9H-fluoren-9-ylidene)bis-
CAS Number: 15499-84-0
Product Number: AG001NIZ(AGN-PC-0JU3GZ)
Synonyms:
MDL No:
Molecular Formula: C25H20N2
Molecular Weight: 348.4397

Identification/Properties

Properties
MP:
237-239 °C
BP:
535.2 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
348.449g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
348.163g/mol
Monoisotopic Mass:
348.163g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
455
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-H312-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4′-(9-Fluorenylidene)dianiline, often referred to as FFD, is a versatile compound used in various chemical synthesis applications. This unique molecule possesses a central fluorene core structure, flanked by amino groups on either side, making it an ideal building block for the creation of complex organic compounds.In chemical synthesis, 4,4′-(9-Fluorenylidene)dianiline serves as a key reagent in the formation of polymeric materials, such as conducting polymers and functionalized coatings. Its rigid fluorene backbone provides enhanced stability and structural integrity to the resulting materials, making them suitable for a range of industrial applications.Additionally, FFD is commonly employed in the synthesis of novel fluorescent dyes and optical materials due to its fluorescence properties. By incorporating this compound into the molecular structure of dyes and materials, researchers can tailor their optical and electronic properties for various specialized applications, including sensors, OLEDs, and biological imaging.Moreover, the presence of amino groups in 4,4′-(9-Fluorenylidene)dianiline enables it to participate in selective functionalization reactions, allowing chemists to introduce specific chemical functionalities at precise positions within a molecule. This versatility makes FFD a valuable tool in the design and synthesis of customized organic compounds with tailored properties for diverse applications.Overall, 4,4′-(9-Fluorenylidene)dianiline plays a crucial role in advancing the field of chemical synthesis by enabling the creation of innovative materials with enhanced performance characteristics and functionality. Whether used in polymer synthesis, fluorescent dye development, or functional group manipulation, this compound offers a wide range of possibilities for researchers and industrial applications alike.