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6-Chloro-5-(2-chloroethyl)oxindole CAS:118289-55-7

6-Chloro-5-(2-chloroethyl)oxindole is a synthetic compound that belongs to the oxindole class of molecules, which are known for their diverse biological activities. The presence of chlorine substituents at specific positions enhances its chemical reactivity and influences its pharmacological properties. This compound has garnered attention in medicinal chemistry for its potential applications in drug development, particularly as a scaffold for designing therapeutics targeting various diseases. Its structural features allow for modifications that may enhance efficacy or selectivity, making it a promising candidate for further exploration in pharmaceutical research.


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Application and Effect:

6-Chloro-5-(2-chloroethyl)oxindole, with the molecular formula C10H8Cl2N2O, represents an intriguing member of the oxindole family, characterized by its bicyclic structure comprising an indole and a carbonyl group. Its unique arrangement, featuring chlorine substituents, contributes to its distinct properties and potential applications in medicinal chemistry. The two chlorine atoms, located at the 6 and 5 positions, introduce significant electron-withdrawing characteristics, which can modulate the compound's reactivity and interaction with biological targets. The oxindole scaffold has been extensively studied due to its wide array of biological activities, including anti-inflammatory, analgesic, and anticancer effects. The introduction of a chloroethyl side chain at position 5 expands the scope of potential pharmacological interactions, allowing for the development of derivatives that may exhibit enhanced therapeutic profiles. Research indicates that compounds with similar structures can target key enzymes and receptors involved in disease pathways, suggesting that 6-chloro-5-(2-chloroethyl)oxindole could serve as a promising lead compound. Moreover, the ability to functionalize the oxindole ring allows for fine-tuning of the compound’s physicochemical properties, impacting its solubility, bioavailability, and metabolic stability. As such, this compound provides a versatile platform for the design of novel drugs aimed at treating various conditions, ranging from cancer to neurological disorders. In addition to its therapeutic potential, the study of 6-chloro-5-(2-chloroethyl)oxindole contributes to understanding structure-activity relationships (SAR) in oxindoles. By elucidating how different substitutions affect biological activity, researchers can optimize new candidates for clinical use. In conclusion, 6-chloro-5-(2-chloroethyl)oxindole stands out as a compelling compound in drug discovery, emphasizing the significance of oxindole derivatives in developing innovative therapeutic agents tailored to combat complex diseases.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C10H9Cl2NO
Assay 99%
Appearance white powder
CAS No.  118289-55-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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