cas 172078-40-9|| where to buy 6-Chloro-1H-indol-5-ol

Nombre del producto:6-Chloro-1H-indol-5-ol

IUPAC Name:6-chloro-1H-indol-5-ol

: CAS：172078-40-9; Fórmula molecular：C8H6ClNO; Pureza：95%

: Número de catálogo：CM238934; Peso molecular：167.59

Unidad de embalaje	Stock disponible	Precio($)
CM238934-100mg	in stock	ǕƻȌ
CM238934-250mg	in stock	ȷƱȦ

Consulta: sales@chemenu.com

Sólo para uso en I+D..

Formulario de consulta

Nombre químico

Número CAS

Cantidad*

Especificaciones requeridas*
(% de ensayo, grado de material, etc.)

Nombre de contacto*

Correo electrónico de contacto*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 172078-40-9 regularly via the above email.

Notas adicionales

Verification code*

refresh

Detalles del producto

: Núm. De CAS :172078-40-9; Fórmula molecular:C8H6ClNO; Punto de fusión:-; Código de sonrisas:OC1=CC2=C(NC=C2)C=C1Cl; Densidad:

: Número de catálogo:CM238934; Peso molecular:167.59; Punto de ebullición:; Nº Mdl:; Almacenamiento:

Category Infos

: Indoles; Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.; indole company; As a indole company,we sincerely welcome the new and old friends from home and abroad to synergize with our company and share the benefits and opportunities.

Column Infos

: Indoles

Product Other Information

Product Overview	6-Chloro-1H-indol-5-ol is a chemical compound that has been widely studied for its potential applications in scientific research. This compound is a derivative of indole, a naturally occurring organic compound that is found in many plants and animals. 6-Chloro-1H-indol-5-ol has been shown to have a range of interesting properties, including potential anti-cancer and anti-inflammatory effects.
Synthesis and Application	The synthesis of 6-Chloro-1H-indol-5-ol involves the reaction of 5-hydroxyindole with thionyl chloride and hydrogen chloride gas. This reaction produces 6-Chloro-1H-indol-5-ol as a white or off-white powder. This synthesis method has been used in many studies to produce 6-Chloro-1H-indol-5-ol for use in scientific research. 6-Chloro-1H-indol-5-ol has been studied for its potential applications in scientific research. One area of research has focused on the potential anti-cancer effects of this compound. Studies have shown that 6-Chloro-1H-indol-5-ol may be able to inhibit the growth of cancer cells and induce apoptosis, or programmed cell death, in cancer cells. Other studies have explored the potential anti-inflammatory effects of this compound, which may make it useful in the treatment of inflammatory diseases such as rheumatoid arthritis.
Future Directions	There are many potential future directions for research on 6-Chloro-1H-indol-5-ol. One area of research could focus on further exploring the potential anti-cancer effects of this compound. Additionally, researchers could investigate the potential anti-inflammatory effects of 6-Chloro-1H-indol-5-ol in more detail. Other future directions could include exploring the mechanism of action of this compound and investigating its potential use in combination with other drugs or therapies. Overall, there is still much to learn about the potential applications of 6-Chloro-1H-indol-5-ol in scientific research.