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CAS:879713-65-2 | 7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole

CAS:879713-65-2 | 7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole

Molecular Formula:C15H14BrN
Molecular Weight:288.18
Purity:97%
Package:250mg 1g 5g
Worldwide Delivery
Made in China

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Product Introduction

 

Introduction of CAS:879713-65-2 | 7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole

 

The compound can be used as a novel nanocarrier-based near-infrared optical probe for in-vivo tumor imaging . This suggests potential applications in the field of medical imaging.

 

Specification of CAS:879713-65-2 | 7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole

 

ITEMS

SPECIFICATION

Purity

97%

Boiling point

382.5±42.0 °C(Predicted)

Density

1.38

Storage condition

Sealed in dry,Room Temperature

 

Research Application of CAS:879713-65-2 | 7-Bromo-1,1,2-trimethyl-1H-benzo[e]indole

Fluorescent Building Blocks

Application : Synthesis of novel fluorescent building blocks.

Method : Reaction with acrylic acid and derivatives for preparing benzo[e]pyrido[1,2-a]indole derivatives.

Properties : Studied using UV–vis and fluorescence spectroscopy (Steponavičiūtė et al., 2014).

Bioactive Aromatic Heterocyclic Macromolecules

Application : Creation of bioactive molecules for potential biological activities.

Method : Modification with monosaccharides to synthesize mono and di-saccharides derivatives.

Properties : Confirmed using spectroscopy methods including NMR, showing antibacterial and antifungal activities (MAHMOOD, Salman, & Abd, 2022).

Optical Properties and Synthesis

Application : Study of optical properties.

Method : Alkylation followed by treatment with acetic acid.

Properties : Analyzed through NMR and UV–Vis and fluorescence spectroscopy (Ščerbetkaitė et al., 2017).

Photopolymerisation Photoinitiators

Application : Radical polymerisation of a system containing trimethylolpropane triacrylate under visible light.

Method : Synthesis of potential initiators based on benz[cd]indol-2(1H)-one dye.

Properties : Demonstrated the ability to act as triplet sensitisers and hydrogen donors in the photopolymerisation process (Strzelczyk, Michalski, & Podsiadły, 2016).

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