structure of N-([1,1'-biphenyl]-4-yl)-9-phenyl-9H-carbazol-3-amine

N-([1,1'-biphenyl]-4-yl)-9-phenyl-9H-carbazol-3-amine

CAS No.: 1002762-60-8
M. Wt: 410.50900
M. Fa: C30H22N2
InChI Key: SWTKZXWNEZJKNY-UHFFFAOYSA-N
Appearance: Yellow Solid

Names and Identifiers of 1002762-60-8

CAS Number

1002762-60-8

IUPAC Name

9-phenyl-N-(4-phenylphenyl)carbazol-3-amine

InChI

InChI=1S/C30H22N2/c1-3-9-22(10-4-1)23-15-17-24(18-16-23)31-25-19-20-30-28(21-25)27-13-7-8-14-29(27)32(30)26-11-5-2-6-12-26/h1-21,31H

InChIKey

SWTKZXWNEZJKNY-UHFFFAOYSA-N

Canonical SMILES

C1=CC=C(C=C1)C2=CC=C(C=C2)NC3=CC4=C(C=C3)N(C5=CC=CC=C54)C6=CC=CC=C6

Physical and chemical properties of 1002762-60-8

Boiling Point

632.8±47.0 °C(Predicted)

Density

1.14±0.1 g/cm3(Predicted)

Exact Mass

410.17800

LogP

8.26730

Molecular Formula

C30H22N2

Molecular Weight

410.50900

PSA

16.96000

Applications of 1002762-60-8

N-([1,1'-biphenyl]-4-yl)-9-phenyl-9H-carbazol-3-amine has diverse applications in:

  • Organic Electronics: It serves as a hole transport material in OLEDs, enhancing device efficiency.
  • Photovoltaics: The compound is used in organic solar cells to improve efficiency and stability.
  • Medicinal Chemistry: It acts as a building block for synthesizing pharmaceuticals and bioactive molecules.
  • Material Science: Utilized in developing new materials with unique electronic and optical properties.

Interaction Studies of 1002762-60-8

The compound's mechanism of action primarily revolves around charge transport in electronic devices. It facilitates the movement of holes, thereby improving the efficiency of organic electronic devices. Additionally, it interacts with specific molecular targets that enhance performance in charge transfer and energy conversion pathways.

Biological Activity of 1002762-60-8

While specific biological activities of N-([1,1'-biphenyl]-4-yl)-9-phenyl-9H-carbazol-3-amine have not been extensively documented, compounds with similar structures often exhibit various biological effects. These may include anti-cancer properties and activity against certain pathogens. Further research is necessary to elucidate its potential pharmacological effects.

Physical sample testing spectrum (NMR) of 1002762-60-8

Physical sample testing spectrum (NMR) of 1002762-60-8