Nom du produit:7-Nitro-1H-indole-3-carbonitrile

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

CAS:165669-10-3
Formule moléculaire:C9H5N3O2
Pureté:95%+
Numéro de catalogue:CM235824
Poids moléculaire:187.16

Unité d'emballage Stock disponible Prix($) Quantité
CM235824-1g 1-2 Weeks ƿŹǙ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:165669-10-3
Formule moléculaire:C9H5N3O2
Point de fusion:-
Code SMILES:N#CC1=CNC2=C1C=CC=C2[N+]([O-])=O
Densité:
Numéro de catalogue:CM235824
Poids moléculaire:187.16
Point d'ébullition:
N° Mdl:
Stockage:

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
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Product Other Information

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.