4,5-Dicyanoimidazole丨CAS 1122-28-7

4,5-Dicyanoimidazole丨CAS 1122-28-7
Product Introduction:
Catalog No.: SS115621
CAS No.: 1122-28-7
Purity(HPLC): 99% min
Product Name: 4,5-Dicyanoimidazole
Molecular Formula: C5H2N4
Molecular Weight: 118.09
Synonym(s): 1H-Imidazole-4,5-dicarbonitrile; DCI
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Technical Parameters
Description

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Specifications of 4,5-Dicyanoimidazole丨CAS 1122-28-7

 

Appearance

Off-white to white powder

Purity (HPLC)

99% min

Melting Point

170°C to 178°C

Water

0.5% max

 

Transport Information of 4,5-Dicyanoimidazole丨CAS 1122-28-7

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2933290090

Stability & Reactivity

The product is chemically stable under standard ambient conditions (room temperature).

Storage

Tightly closed. Store in a closed, dry, ventilated place

Condition to Avoid

Avoid formation of dust and aerosols

Package

 

4,5-Dicyanoimidazole丨CAS 1122-28-7 (DCI) is an organic compound featuring a cyano group (-C≡N) attached to the imidazole ring at the 4 and 5 positions. It is primarily utilized in the fields of organic chemistry, material science, and pharmaceutical development due to its unique electronic properties and ability to act as a nucleophilic reagent.

 

Key Applications of 4,5-Dicyanoimidazole丨CAS 1122-28-7

 

1. Organic Synthesis
● Electrophilic Substitution Reactions: 4,5-Dicyanoimidazole丨CAS 1122-28-7 can participate in nucleophilic substitution reactions and is used as a reagent for introducing cyano groups into various organic compounds, helping synthesize complex heterocyclic structures and functionalized imidazoles.
● Synthesis of Heterocycles: The imidazole ring in 4,5-dicyanoimidazole can act as a precursor for heterocyclic chemistry, aiding in the creation of complex, nitrogen-containing compounds that are useful in both medicinal chemistry and material science.
2. Pharmaceutical Research
● Potential Antimicrobial and Antiviral Properties: 4,5-Dicyanoimidazole has shown potential as a lead compound for developing antimicrobial and antiviral agents due to the biological activity imparted by the imidazole ring and the electron-withdrawing cyano groups. It is a candidate for further exploration in the design of drug candidates for various diseases, especially in areas where drug resistance is a concern.
● Medicinal Chemistry: The compound has been studied for its cytotoxic and antitumor activities, making it a potential candidate for the development of anticancer agents. Its structure can be modified to enhance its selectivity and efficacy against cancer cells.
3. Material Science
● Molecular Electronics: Due to its unique electronic properties, 4,5-dicyanoimidazole is used in the development of molecular electronics, where its ability to donate electrons can be exploited in devices such as organic semiconductors and light-emitting diodes (OLEDs).
● Polymer Chemistry: The cyano groups in 4,5-dicyanoimidazole can be used in the creation of polymeric materials that exhibit desirable electronic properties, such as conductivity and stability. This makes it useful in the production of organic electronic devices.
4. Catalysis
● Catalyst in Organic Reactions: 4,5-dicyanoimidazole can act as a catalyst in certain organic reactions due to its nucleophilic nature. It can facilitate addition reactions and substitution reactions by activating other reagents or substrates, especially in the synthesis of heterocyclic compounds.
● Organocatalysis: It has potential in organocatalysis, where it can catalyze molecular transformations in a green chemistry context, helping reduce reliance on metal-based catalysts.
5. Dye and Pigment Industry
● Dye Synthesis: 4,5-Dicyanoimidazole is used as a precursor in the synthesis of certain dyes and pigments, especially those used in organic light-emitting diodes (OLEDs), and other electronic devices. The functionalization of the imidazole ring with the cyano groups gives the compound unique optical properties, such as absorption and fluorescence.

 

Benefits of 4,5-Dicyanoimidazole丨CAS 1122-28-7

 

1. Versatile Reactivity
● Nucleophilic Character: 4,5-Dicyanoimidazole丨CAS 1122-28-7 possesses significant nucleophilic reactivity, allowing it to participate in various synthetic transformations, including substitution, addition, and condensation reactions.
● Facilitating Functionalization: The cyano groups in the structure can undergo further chemical modification, making this compound a valuable intermediate in organic synthesis for functionalizing other molecules.
2. Broad Range of Applications
● Multi-Industry Use: Its application extends from pharmaceutical development to electronic materials and catalysis, highlighting its flexibility across industries. Whether for drug development, polymer engineering, or synthesis of novel materials, 4,5-dicyanoimidazole plays a key role in many advanced chemical processes.
3. Enhanced Chemical Stability
● Stability in Various Conditions: The cyano groups in 4,5-dicyanoimidazole provide the compound with chemical stability, allowing it to be used in a wide range of environments without significant degradation. This makes it reliable for use in harsh chemical reactions and under varying temperatures and conditions.
4. Potential for Green Chemistry
● Mild Reaction Conditions: When used as a catalyst or reagent in organic reactions, 4,5-dicyanoimidazole can operate under mild conditions, which can contribute to green chemistry approaches by reducing the need for high temperatures, pressures, or toxic reagents.
5. Tunable Properties
● Functional Group Modification: The structure of 4,5-dicyanoimidazole can be modified by changing the substituents on the imidazole ring, allowing for the tailoring of properties like solubility, reactivity, and biological activity. This makes it highly adaptable for use in various customized chemical applications.

 

Conclusion

 

4,5-Dicyanoimidazole丨CAS 1122-28-7 is a versatile organic compound with a wide range of applications in organic synthesis, pharmaceutical research, material science, catalysis, and even the dye industry. Its unique cyano-substituted imidazole structure allows for diverse reactivity, making it valuable in the synthesis of heterocyclic compounds, the development of electronic materials, and as a potential drug candidate.
Its stability, versatility, and potential for green chemistry approaches further contribute to its usefulness in various industries. Whether employed as a catalyst, nucleophile, or precursor for other functional materials, 4,5-dicyanoimidazole has established itself as a critical reagent for both academic research and industrial applications.

 

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