Nombre del producto:2-chloro-5-iodo-1H-benzo[d]imidazole

IUPAC Name:2-chloro-5-iodo-1H-1,3-benzodiazole

CAS:256518-97-5
Fórmula molecular:C7H4ClIN2
Pureza:95%
Número de catálogo:CM131782
Peso molecular:278.48

Unidad de embalaje Stock disponible Precio($) Cantidad
CM131782-250mg in stock Ůǟ
CM131782-1g in stock ƴǸƴ
CM131782-5g in stock ijǟǸƴ

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :256518-97-5
Fórmula molecular:C7H4ClIN2
Punto de fusión:-
Código de sonrisas:IC1=CC=C2NC(Cl)=NC2=C1
Densidad:
Número de catálogo:CM131782
Peso molecular:278.48
Punto de ebullición:409.7°C at 760 mmHg
Nº Mdl:MFCD11044655
Almacenamiento:Keep in dark place, inert atmosphere, store at 2-8°C.

Category Infos

Benzimidazoles
Benzimidazole is a benzo derivative of imidazole. It is a kind of bicyclic aromatic organic compounds, which is formed by fusing a six-membered benzene ring and five-membered imidazole at positions 4 and 5 of imidazole ring. It is an important pharmacophore of many biologically active heterocyclic compounds with various pharmacological activities. Benzimidazoles and their derivatives have developed into dynamic heterocyclic systems due to their potency in a variety of biologically active compounds such as anticancer, bactericidal and antiviral drugs. Benzimidazoles are a class of therapeutic motifs with broad relevance in medicinal chemistry.

Related Products



Product Other Information

Product Overview 2-chloro-5-iodo-1H-benzo[d]imidazole, also known as CIBI, is an organic compound that has a wide range of applications in the scientific research field. It is a heterocyclic system containing an imidazole ring, a benzene ring, and two halogens. This compound has been studied extensively for its unique properties and has been found to be useful for a variety of scientific research applications.
Synthesis and Application The synthesis of 2-chloro-5-iodo-1H-benzo[d]imidazole has been studied extensively, and a variety of methods have been developed. The most common method involves the reaction of 2-chloro-5-iodobenzaldehyde with 1,3-diaminopropane in the presence of a base. This reaction produces 2-chloro-5-iodo-1H-benzo[d]imidazole in high yields and is relatively simple to perform. Other methods, such as the reaction of 2-chloro-5-iodobenzaldehyde with hydrazine hydrate, have also been developed, but these are less commonly used. 2-chloro-5-iodo-1H-benzo[d]imidazole has a wide range of applications in the scientific research field. It is widely used as a fluorescent label for the detection and imaging of biomolecules, as it has strong fluorescence properties. It has also been used as a reagent for the synthesis of a variety of heterocyclic compounds, including quinolines and indoles. Additionally, it has been used as a catalyst for a variety of organic reactions, such as the Heck reaction.
Future Directions There are a variety of potential future directions for the use of 2-chloro-5-iodo-1H-benzo[d]imidazole. One potential direction is the development of new synthetic methods for the production of 2-chloro-5-iodo-1H-benzo[d]imidazole. Additionally, further research into the biochemical and physiological effects of 2-chloro-5-iodo-1H-benzo[d]imidazole may lead to new applications in the field of medicine. Additionally, further research into the fluorescence properties of 2-chloro-5-iodo-1H-benzo[d]imidazole may lead to new methods for the detection and imaging of biomolecules. Finally, further research into the reactivity of 2-chloro-5-iodo-1H-benzo[d]imidazole may lead to new methods for the synthesis of heterocyclic compounds.