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7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole is a specialized, complex chemical compound that falls under the class of organic compounds known as benzindoles. This class of compounds is characterized by a benzene ring fused to an indole. The structure of 7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole is further decorated with additional substituents such as bromine and methyl groups at certain positions. These additions and the general structure of the compound lend to its unique physical and chemical properties, which include its solubility, melting point, and possible reactivity with other substances.

879713-65-2

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879713-65-2 Usage

Uses

Used in Pharmaceutical Industry:
7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole is used as a potential pharmaceutical compound for its unique chemical structure and properties. Its specific applications may include the development of new drugs or the enhancement of existing ones, given its potential reactivity with other substances and its distinct physical and chemical properties.
Used in Chemical Research:
7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole is used as a research compound in the field of organic chemistry. Its unique structure and properties make it a valuable subject for studying the effects of different substituents on the overall characteristics of benzindole compounds, which can contribute to the advancement of chemical knowledge and the development of new compounds with specific applications.
Used in Material Science:
7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole is used as a component in the development of new materials. Its unique properties, such as solubility and melting point, may be harnessed to create materials with specific characteristics, such as improved stability or enhanced reactivity, which can be applied in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 879713-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,7,1 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 879713-65:
(8*8)+(7*7)+(6*9)+(5*7)+(4*1)+(3*3)+(2*6)+(1*5)=232
232 % 10 = 2
So 879713-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H14BrN/c1-9-15(2,3)14-12-6-5-11(16)8-10(12)4-7-13(14)17-9/h4-8H,1-3H3

879713-65-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromo-1,1,2-trimethylbenzo[e]indole

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:879713-65-2 SDS

879713-65-2Upstream product

879713-65-2Downstream Products

879713-65-2Relevant academic research and scientific papers

Polymethine dyes-loaded solid lipid nanoparticles (SLN) as promising photosensitizers for biomedical applications

Barbero, Nadia,Barolo, Claudia,Chinigò, Giorgia,Fiorio Pla, Alessandra,Gasco, Paolo,Gilardino, Alessandra,Gonzalez-Paredes, Ana,Visentin, Sonja

, (2022/02/01)

Polymethine dyes (PMD) have proved to be excellent candidates in the biomedical field for potential applications in both diagnostic and therapeutic. However, PMD application in biomedicine is hindered by their poor solubility and stability in physiological conditions. Therefore, the incorporation of these dyes in nanosystems could be important to prevent the formation of dye aggregates in aqueous environment and to protect their photophysical characteristics. In the present work, two PMD based on the benzoindolenine ring (bromine benzo-cyanine-C4 and bromine benzo-squaraine-C4) were incorporated into Solid Lipid Nanoparticles (SLN) to solubilize and stabilize them in aqueous solutions. Obtained SLN showed a high incorporation efficiency for both PMD (≈90%) and not only preserved their spectroscopic properties in the NIR region even under physiological conditions but also improved them. Viability assays showed good biocompatibility of both empty and loaded nanocarriers while the cellular uptake and intracellular localization showed the effective internalization in MCF-7 cells, with a partial mitochondrial localization for CY-SLN. Moreover, in vitro phototoxicity assay showed that cyanine loaded-SLN (CY-SLN) is more photoactive than the free dye.

4,5-benzoindole compound and light-emitting application thereof

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Paragraph 0048; 0049; 0050, (2018/09/08)

The invention provides a 4,5-benzoindole compound with a structural formula shown in the description. The 4,5-benzoindole compound has better thermal stability, high light emitting efficiency and highlight-emitting purity and can be applied to the fields of organic light-emitting devices, organic solar cells, perovskite batteries, organic thin-film transistors or organic light sensors. The invention also provides an organic light-emitting device. The device comprises an anode, a cathode and organic layers, the organic layers contain at least one layer of a light emitting layer, a hole injection layer, a hole transmission layer, an exciton barrier layer and an electronic transmission layer, and at least one layer of the organic layers contains the 4,5-benzoindole compound shown in a structural formula I. The organic light-emitting device prepared from the 4,5-benzoindole compound has the advantages of good light emitting efficiency, excellent color purity and long service life.

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