cas 165669-10-3|| where to buy 7-Nitro-1H-indole-3-carbonitrile

Product Name:7-Nitro-1H-indole-3-carbonitrile

IUPAC Name:7-nitro-1H-indole-3-carbonitrile

Packing Unit	Available Stock	Price($)	Quantity
CM235824-1g	1-2 Weeks	ƙȷŴ

For R&D use only.

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: CAS NO:165669-10-3; Molecular Formula:C9H5N3O2; Melting Point:-; Smiles Code:N#CC1=CNC2=C1C=CC=C2[N+]([O-])=O; Density:

: Catalog Number:CM235824; Molecular Weight:187.16; Boiling Point:; MDL No:; Storage:

: 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.

Product Overview	7-Nitro-1H-indole-3-carbonitrile is a heterocyclic compound that contains a nitrogen atom in its ring structure.
Physical Properties	It is poor solubility in water and its potential to form aggregates in solution.
Chemical Properties	The compound is stable and can be easily synthesized. It has also been shown to exhibit low toxicity and high selectivity towards cancer cells.
Synthesis and Application	The compound has been used as a fluorescent probe for the detection of DNA damage. It has also been used as a photosensitizer in photodynamic therapy for the treatment of cancer. Moreover, the compound has been studied for its potential as an inhibitor of protein kinases and as a modulator of ion channels.
Future Directions	One direction is to explore the potential of the compound as a fluorescent probe for the detection of DNA damage in living cells. Another direction is to investigate the potential of the compound as a photosensitizer in photodynamic therapy for the treatment of cancer. Additionally, further studies are needed to understand the mechanism of action of the compound and its potential as an inhibitor of protein kinases and as a modulator of ion channels.