Description
4,4′-Bis(3-bromo-9H-carbazol-9-yl)biphenyl (CAS No. 848086-93-1) is a high-purity brominated carbazole derivative with the molecular formula C36H22Br2N2. This compound features a biphenyl core symmetrically functionalized with two 3-bromo-9H-carbazole groups, making it an excellent building block for organic electronic materials. Its rigid, conjugated structure and bromine substituents enable further functionalization via cross-coupling reactions, such as Suzuki or Ullmann couplings. Ideal for researchers developing organic semiconductors, OLEDs, or photovoltaic materials, this product is supplied with comprehensive analytical data (HPLC, NMR, MS) to ensure quality and reproducibility. Store under inert conditions to maintain stability.
Properties
- CAS Number: 848086-93-1
- Complexity: 795
- IUPAC Name: 3-bromo-9-[4-[4-(3-bromocarbazol-9-yl)phenyl]phenyl]carbazole
- InChI: InChI=1S/C36H22Br2N2/c37-25-13-19-35-31(21-25)29-5-1-3-7-33(29)39(35)27-15-9-23(10-16-27)24-11-17-28(18-12-24)40-34-8-4-2-6-30(34)32-22-26(38)14-20-36(32)40/h1-22H
- InChI Key: PIQLSWNMCZTPKJ-UHFFFAOYSA-N
- Exact Mass: 642.01292
- Molecular Formula: C36H22Br2N2
- Molecular Weight: 642.4
- SMILES: C1=CC=C2C(=C1)C3=C(N2C4=CC=C(C=C4)C5=CC=C(C=C5)N6C7=C(C=C(C=C7)Br)C8=CC=CC=C86)C=CC(=C3)Br
- Topological: 9.9
- Monoisotopic Mass: 640.01497
- Synonyms: 848086-93-1, 4,4′-Bis(3-bromo-9H-carbazol-9-yl)biphenyl, 4,4′-Bis(3-bromo-9H-carbazol-9-yl)-1,1′-biphenyl, SCHEMBL26218475, AS-88174, F20845
Application
4,4′-Bis(3-bromo-9H-carbazol-9-yl)biphenyl is widely used as a key intermediate in the synthesis of advanced organic electronic materials. Its brominated carbazole units facilitate polymerization or oligomerization for creating hole-transporting layers in OLED devices. Researchers also employ it to develop thermally activated delayed fluorescence (TADF) emitters due to its rigid, planar structure. Additionally, it serves as a precursor for phosphorescent host materials in optoelectronic applications.
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