CAS 15861-24-2
:Indol-5-carbonitrilo
- 1H-indole-5-carbonitrile
- 5-Cyano Indole
- 5-Cyano-1H-indole
- Indole-5-carbonitrile
- 1H-Indole-5-carbonitrile, hydrate (1:2)
- 5-Cyanoindole
Indole-5-carbonitrile, 98+%
CAS:Reactant used for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction, preparation of novel PPAR/ dual agonists for potential treatment of metabolic syndrome and IDDM, chemo selective and regioselective preparation of benzoyl indoles, 4
Fórmula:C9H6N2Pureza:98+%Forma y color:White to cream to yellow to orange to brown, PowderPeso molecular:142.165-Cyanoindole
CAS:Fórmula:C9H6N2Pureza:≥ 98.0%Forma y color:Off-white to yellow powderPeso molecular:142.161H-Indole-5-carbonitrile
CAS:1H-Indole-5-carbonitrileFórmula:C9H6N2Pureza:≥95%Forma y color: light brown to brown solidPeso molecular:142.16g/mol5-Cyanoindole
CAS:Fórmula:C9H6N2Pureza:>98.0%(GC)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular:142.165-Cyanoindole
CAS:5-Cyanoindole is a hydrophobic molecule that has been shown to have an inhibitory effect on the trifluoroacetic acid-induced fluorescence in the presence of chloride ions. It is also able to bind peptides and has been used as an antimicrobial peptide. 5-Cyanoindole can be synthesized electrochemically or by electrochemical impedance spectroscopy. The synthesis of 5-cyanoindole can be achieved through a Friedel-Crafts reaction, followed by a hydrolysis with hydrogen peroxide and then a reduction with sodium borohydride.
!-- END OF PRODUCT DESCRIPTION -->Fórmula:C9H6N2Forma y color:White PowderPeso molecular:142.16 g/mol5-Cyanoindole
CAS:5-Cyanoindole is a versatile building block that can be used in the synthesis of complex compounds.Fórmula:C9H6N2Peso molecular:142.16 g/molRef: 3D-C-8840
1kgA consultar100gA consultar250gA consultar500gA consultar2500gA consultar-Unit-ggA consultar5-Cyanoindole
CAS:Producto controladoApplications Inhibitor of enzyme.
Fórmula:C9H6N2Forma y color:NeatPeso molecular:142.16










