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CAS:12217-79-7 | Disperse Blue 56

CAS:12217-79-7 | Disperse Blue 56

Molecular Formula:C14H9BrN2O4
Molecular Weight:349.14
EINECS:235-401-1
Package:100g 500g 1kg
Worldwide Delivery
Made in China

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Product Introduction

Introduction of CAS:12217-79-7 | Disperse Blue 56

 

Anthracene derivatives, including those related to 9,10-Anthracenedione, play a prominent role in various fields, such as material chemistry and medicinal applications. These compounds have been used in optical, electronic, and magnetic switches, as well as in probing DNA cleavage.

 

Specification of CAS:12217-79-7 | Disperse Blue 56

 

ITEMS

SPECIFICATION

Density

1.4410 (rough estimate)

Boiling point

129°C (rough estimate)

Refractive index

1.6800 (estimate)

 

Research Application of CAS:12217-79-7 | Disperse Blue 56

 

Marine-Derived Fungi Derivatives

Anthraquinones and their derivatives, including structures similar to 9,10-Anthracenedione, have been identified in marine-derived filamentous fungi. These compounds are noted for their structural diversity and biological activities, attracting attention from industries such as pharmaceuticals, clothes dyeing, and food colorants. Their effects on human health are under investigation, suggesting potential roles or effects that are strongly discussed among scientists. Marine microorganisms appear as promising resources for identifying new therapeutic drug candidates or daily additives, highlighting the importance of anthraquinoid compounds in various applications (Fouillaud et al., 2016).

Treatment of Multiple Sclerosis

Research has explored anthracenedione agents, including derivatives structurally related to 9,10-Anthracenedione, for treating multiple sclerosis (MS). These studies have aimed to develop more efficacious drugs with fewer adverse effects, highlighting the need for effective MS treatment. Chromophore modification of anthracenedione agents has yielded a novel class of DNA binding agents with potential for reduced cardiotoxicity, suggesting the significance of such compounds in medical applications (Koffman et al., 2016).

Chemical Carcinogenesis

Studies have also examined the role of compounds structurally related to 9,10-Anthracenedione in experimental carcinogenesis, particularly in the oral cavity and submandibular salivary glands. The effects of related compounds on experimental carcinogenesis have shown varying results, from enhancing tumor induction to having no significant effect, indicating the complex interactions of such compounds with biological systems (Sabes et al., 1963).

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