3682-85-7

Basic information

• Product Name: 5,10-Dihydroindolo[3,2-b]indole
• Synonyms: 5,10-Dihydroindolo[3,2-b]indole;Indolo[3,2-b]indole,5,10-dihydro-
• CAS NO: 3682-85-7
• Molecular Formula: C₁₄H₁₀N₂
• Molecular Weight: 206.2426
• Mol File: 3682-85-7.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 483.4±18.0 °C(Predicted)
• Appearance: /
• Density: 1.389±0.06 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 16.70±0.30(Predicted)
• CAS DataBase Reference: 5,10-Dihydroindolo[3,2-b]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5,10-Dihydroindolo[3,2-b]indole(3682-85-7)
• EPA Substance Registry System: 5,10-Dihydroindolo[3,2-b]indole(3682-85-7)

Safety Data

• Hazardous Substances Data: 3682-85-7(Hazardous Substances Data)

Usage

General Description

5,10-Dihydroindolo[3,2-b]indole, also known as DHII, is a heterocyclic compound with a unique indole structure. It is synthesized through the Fischer indole synthesis and has been studied for its potential pharmaceutical applications, particularly in the area of cancer treatment. DHII has been found to exhibit cytotoxic and antiproliferative effects on cancer cells, making it a promising candidate for the development of new anticancer drugs. It has also been investigated for its potential use in the treatment of neurological disorders, due to its ability to modulate serotonin receptors. Additionally, DHII has shown potential as a fluorescent probe for the selective detection of metal ions. Overall, the compound's diverse potential applications make it an interesting target for further research in the fields of medicinal chemistry and material science.

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Relevant articles and documents

Double anchor indolo[3,2-: B] indole-derived metal-free dyes with extra electron donors as efficient sensitizers for dye-sensitized solar cells

Two new di-acceptors metal-free organic dyes based on indolo[3,2-b]indole donor backbone with extra electron donors were designed, synthesized, and applied for dye-sensitized solar cells (DSSCs). In this study, the effect of the additional donors was inve

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

A heterocyclic compound and an organic light-emitting device including the heterocyclic compound, the heterocyclic compound being represented by Formula 1:

Dicyanovinyl-substituted indolo[3,2-b] indole derivatives: Low-band-gap π-conjugated molecules for a single-component ambipolar organic field-effect transistor

A series of low-band-gap π-conjugated molecules comprising N,N′-dihexylindolo[3,2-b]indole as an electron donor (D) and dicyanovinyl as an electron acceptor (A) with A-π-D-π-A architecture have been designed and synthesized to fabricate a single-component