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CAS:78637-85-1 | 3,4-Diaminothiophene Dihydrobromide

CAS:78637-85-1 | 3,4-Diaminothiophene Dihydrobromide

Molecular Formula:C4H6N2S
Molecular Weight:114.17
Purity:98%
Package:100mg 250mg 1g
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Made in China

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Product Introduction

Introduction of CAS:78637-85-1 | 3,4-Diaminothiophene dihydrobromide

 

3,4-Diaminothiophene (3,4-DAT) is an organic compound containing a thiophene ring with two amino groups. It is a colorless solid that is soluble in polar organic solvents. It is used in the synthesis of various organic compounds and has a wide range of scientific research applications. This article will discuss the synthesis methods, scientific research applications, mechanism of action, biological activity, biochemical and physiological effects, pharmacodynamics, advantages and limitations for lab experiments, and future directions of 3,4-DAT.

 

Specification of CAS:78637-85-1 | 3,4-Diaminothiophene dihydrobromide

 

ITEMS

SPECIFICATION

Purity

98%

Melt point

150 °C

Boiling point

362.6±22.0 °C(Predicted)

Density

1.367±0.06 g/cm3(Predicted)

Storage condition

under inert gas (nitrogen or Argon) at 2–8 °C

 

Related Articles of CAS:78637-85-1 | 3,4-Diaminothiophene dihydrobromide

 

Electrophilic Reactivity and Carbon-Carbon Coupling

Studies on 3,4-Diaminothiophene have revealed its strong nucleophilic character at the carbon positions, demonstrating its potential for fast carbon-carbon coupling reactions. This characteristic opens possibilities for its use in various chemical syntheses (Terrier et al., 2010).

 

Synthesis of Thieno[3,4-b]pyrazines

Methods have been developed for synthesizing 2,3-disubstituted thieno[3,4-b]pyrazines using 3,4-diaminothiophene. These compounds have applications in various fields, including material science and pharmaceuticals (Kenning et al., 2002).

 

Photophysical and Electronic Properties

Research on thiophene-centered azomethines derived from 3,4-diaminothiophene has explored their photophysical and electronic properties. These findings are relevant for the development of materials in optoelectronics and photonics (Tokárová et al., 2020).

 

Electrochemistry of Conjugated Oligothiophenes

Conjugated azomethines consisting of thiophenes prepared from a stable diaminothiophene exhibit significant photophysics and electrochemistry. Their stability and resistance to various chemical processes make them suitable for use in electronics and materials science (Bourgeaux & Skene, 2007).

 

Complexation with Metal Cations

Thiophene derivatives, including those related to 3,4-diaminothiophene, have been studied for their ability to form complexes with metal cations. This research is significant for understanding their potential applications in coordination chemistry and materials science (El-Dossoki, 2008).

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