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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)-

9H-Fluorene, 2,7-dibromo-9,9-didodecyl-

CCCCCCCCCCCCC1(CCCCCCCCCCCC)c2cc(Br)ccc2c2c1cc(Br)cc2 Request for Quotation
Chemical Name: 9H-Fluorene, 2,7-dibromo-9,9-didodecyl-
CAS Number: 286438-45-7
Product Number: AG002VYB(AGN-PC-0LNBVF)
Synonyms:
MDL No: MFCD03427214
Molecular Formula: C37H56Br2
Molecular Weight: 660.6485

Identification/Properties

Properties
MP:
50-55 °C(lit.);
BP:
651.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
660.663g/mol
XLogP3:
17.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
22
Exact Mass:
660.273g/mol
Monoisotopic Mass:
658.275g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
39
Formal Charge:
0
Complexity:
550
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,7-Dibromo-9,9-didodecyl-9H-fluorene is a versatile compound used in chemical synthesis for its unique properties and reactivity. This compound is commonly employed as a building block in the synthesis of organic materials, particularly in the field of organic electronics and materials science. Its bromine functional groups make it a valuable intermediate in the preparation of various functionalized molecules and polymers. In the realm of materials chemistry, 2,7-Dibromo-9,9-didodecyl-9H-fluorene serves as a key precursor for the fabrication of conjugated polymers and organic semiconductors, which find applications in optoelectronic devices such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). Furthermore, its specific structural characteristics contribute to the enhancement of desirable properties such as high thermal stability, efficient charge transport, and tunable electronic properties, making it an essential component in the design and construction of advanced organic materials with tailored functionalities and performance.