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CAS:5007-67-0 | 3.3'.4.4'-TETRA AMINOBENZOPHENONE

CAS:5007-67-0 | 3.3'.4.4'-TETRA AMINOBENZOPHENONE

Molecular Formula:C13H14N4O
Molecular Weight:242.28
EINECS:225-683-4
Package:250mg 1g 5g
Worldwide Delivery
Made in China

Product Introduction

Introduction of CAS:5007-67-0 | 3.3'.4.4'-TETRA AMINOBENZOPHENONE

 

Chemical Reactions Analysis

While the papers do not directly discuss the chemical reactions of methanone, bis(3,4-diaminophenyl)-, they do mention the reactivity of related compounds. For example, the third paper discusses the synthesis of new thieno[2,3-b]-thiophene derivatives, which involve reactions pertinent to heterocyclic chemistry3. These reactions could potentially be adapted to synthesize or modify methanone, bis(3,4-diaminophenyl)-, by applying similar principles of organic synthesis.

 

Physical and Chemical Properties Analysis

The physical properties of a related bisphenyl methanone derivative are characterized in the second paper using AM1 and B3LYP/6-31G* calculations2. These computational methods could be used to predict the physical properties of methanone, bis(3,4-diaminophenyl)-, such as its electronic structure, reactivity, and potential as a material in electronic applications. Additionally, the antibacterial and antifungal activities of the compound in the second paper suggest that methanone derivatives could have bioactive properties, which might also be true for methanone, bis(3,4-diaminophenyl)-.

 

Specification of CAS:5007-67-0 | 3.3'.4.4'-TETRA AMINOBENZOPHENONE

 

ITEMS

SPECIFICATION

Form

Powder or crystalline powder

Color

White to light brown

Solubility

Freely soluble inmethanol

Melt point

70-74 °C (lit.)

Storage condition

Keep in dark place,Inert atmosphere,Room temperature

 

Research Application of CAS:5007-67-0 | 3.3'.4.4'-TETRA AMINOBENZOPHENONE

 

Methanol as a Resource

 

Methane, a closely related compound to methanol produced from methanotrophs' activity on methane, demonstrates the versatility of methanol-related compounds in biotechnological applications. Methanotrophs can convert methane into valuable products such as single-cell proteins, biopolymers, nanotechnology components, methanol, formaldehyde, and lipids. These applications underscore the potential of methanol and related compounds in sustainable production and environmental remediation efforts, highlighting the capacity for generating value while sequestering greenhouse gases (Strong, Xie, & Clarke, 2015).

 

Catalysts in Organic Synthesis

 

A practical synthesis method involving methanone derivatives emphasizes the role of these compounds as intermediates in creating valuable materials such as metal passivators and light-sensitive materials. The process involves the efficient and environmentally benign preparation of 5,5′-Methylene-bis(benzotriazole), showcasing the application of methanone derivatives in green chemistry and organic synthesis (Gu, Yu, Zhang, & Xu, 2009).

 

Renewable Energy and Fuel Cells

 

Methanol, produced from methanone derivatives, plays a significant role in renewable energy technologies, especially in direct methanol fuel cells (DMFCs). The review of methanol crossover in DMFCs highlights the challenges and advancements in utilizing methanol as an efficient fuel source. This application is crucial for the development of clean energy technologies and reducing reliance on fossil fuels (Heinzel & Barragán, 1999).

 

Environmental Monitoring and Remediation

 

Methanol and its derivatives are studied for their role in environmental monitoring and remediation. For example, methanol acts as a chemical marker in assessing the condition of solid insulation in power transformers. This application demonstrates the utility of methanol-related compounds in monitoring and maintaining infrastructure in an environmentally conscious manner (Jalbert, Rodriguez-Celis, Arroyo-Fernández, Duchesne, & Morin, 2019).

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