cas 1366234-02-7|| where to buy 5-Fluoro-6-nitrobenzo[d][1,3]dioxole

Nom du produit:5-Fluoro-6-nitrobenzo[d][1,3]dioxole

IUPAC Name:5-fluoro-6-nitro-2H-1,3-benzodioxole

: CAS：1366234-02-7; Formule moléculaire：C7H4FNO4; Pureté：95%+

: Numéro de catalogue：CM384801; Poids moléculaire：185.11

Unité d'emballage	Stock disponible	Prix($)
CM384801-250mg	in stock	ƻƏň
CM384801-1g	in stock	ƅƻȋ
CM384801-5g	in stock	șƩƻȋ
CM384801-10g	in stock	ƻƏƩƅ

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Détails du produit

: N° CAS:1366234-02-7; Formule moléculaire:C7H4FNO4; Point de fusion:-; Code SMILES:[O-][N+](=O)C1=CC2=C(OCO2)C=C1F; Densité:

: Numéro de catalogue:CM384801; Poids moléculaire:185.11; Point d'ébullition:; N° Mdl:; Stockage:

Category Infos

: Benzodioxolanes

Product Other Information

Product Overview	5-Fluoro-6-nitrobenzo[d][1,3]dioxole, also known as FNBDO, is a chemical compound that has gained significant attention in scientific research due to its unique properties. FNBDO is a heterocyclic compound that contains both a benzene and dioxole ring.
Synthesis Method	The synthesis of 5-Fluoro-6-nitrobenzo[d][1,3]dioxole involves the reaction of 2,4-dinitrophenol with 2,3-difluorophenol in the presence of a catalyst. The resulting intermediate is then treated with sodium hydroxide to form 5-Fluoro-6-nitrobenzo[d][1,3]dioxole.
Chemical Properties	5-Fluoro-6-nitrobenzo[d][1,3]dioxole has the advantages of using in lab experiments is its high reactivity, which allows for the creation of new compounds with potentially useful properties. However, the high reactivity of 5-Fluoro-6-nitrobenzo[d][1,3]dioxole also presents a limitation, as it can be difficult to control reactions and ensure high yields and purity.
Synthesis and Application	It has been used as a fluorescent probe to study protein-ligand interactions, as well as to detect metal ions in biological systems. 5-Fluoro-6-nitrobenzo[d][1,3]dioxole has also been used as a building block for organic synthesis, allowing for the creation of new compounds with potentially useful properties.
Future Directions	One area of interest is the development of new anticancer agents based on 5-Fluoro-6-nitrobenzo[d][1,3]dioxole. Additionally, 5-Fluoro-6-nitrobenzo[d][1,3]dioxole could be used in the development of new antibiotics to combat drug-resistant bacteria. Further research is also needed to fully understand the mechanism of action of 5-Fluoro-6-nitrobenzo[d][1,3]dioxole and its potential applications in various fields of science.