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5-BROMOINDOLINE CAS:22190-33-6

5-Bromoindoline is an organic compound belonging to the indoline family, characterized by the presence of a bromine atom at the 5-position of the indoline framework. This unique substitution enhances its chemical reactivity and introduces distinct properties that may be useful in various applications, including medicinal chemistry and materials science. Indolines are known for their biological activities and are found in several natural products and pharmacologically relevant compounds. The introduction of the bromine substituent can alter the compound’s electronic properties, potentially affecting its interactions with biological targets, making 5-bromoindoline a subject of interest in drug design and development.


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Application and Effect:

5-Bromoindoline is a fascinating member of the indoline class of compounds, which are characterized by a fused bicyclic structure consisting of a benzene ring and a pyrrole-like nitrogen-containing five-membered ring. The presence of a bromine atom at the 5-position contributes notable chemical and physical properties to this compound, influencing its reactivity, solubility, and potential biological activity. Brominated compounds often exhibit enhanced lipophilicity and metabolic stability, making them important in pharmaceutical development. The introduction of the bromine substituent in 5-bromoindoline could modify its interaction with various protein targets, such as receptors and enzymes, providing potential therapeutic benefits. Indolines have been linked to numerous biological activities, including anti-inflammatory, antimicrobial, and anticancer effects. Therefore, 5-bromoindoline may serve as a promising scaffold for the design of novel bioactive molecules. Synthesis of 5-bromoindoline can be achieved through several methods, including electrophilic bromination of indoline or other synthetic pathways involving indole derivatives. The versatility of synthetic strategies allows for the generation of diverse analogs, whereby further functionalization may lead to compounds with tailored properties and enhanced biological activities. Moreover, 5-bromoindoline’s unique structure makes it an attractive candidate for use in materials science and organic electronics. Its ability to form pi-stacking interactions and contribute to charge transport could facilitate the development of advanced materials for optoelectronic devices. In conclusion, 5-bromoindoline represents a multifaceted compound with significant potential across multiple fields, including medicinal chemistry, synthetic organic chemistry, and materials science. Further research into its properties, synthesis, and biological applications could lead to valuable insights and innovations in drug discovery and material development. The exploration of 5-bromoindoline and its derivatives is warranted to fully understand its capabilities and contributions to science.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C8H8BrN
Assay 99%
Appearance white powder
CAS No.  22190-33-6
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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