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383155-01-9

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383155-01-9 Usage

Category

Naphthalene derivatives

Key feature

Fluorine atom at the eighth position of the naphthalenol ring

Potential applications

Pharmaceuticals, agrochemicals, and material science

Unique properties

Increased lipophilicity and bioavailability due to the presence of the fluorine substituent

Importance

Valuable building block in the synthesis of novel molecules

Additional research needed

To explore its full range of properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 383155-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,5 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 383155-01:
(8*3)+(7*8)+(6*3)+(5*1)+(4*5)+(3*5)+(2*0)+(1*1)=139
139 % 10 = 9
So 383155-01-9 is a valid CAS Registry Number.

383155-01-9Downstream Products

383155-01-9Relevant articles and documents

Structural modifications of nile red carbon monoxide fluorescent probe: Sensing mechanism and applications

Klán, Petr,Madea, Dominik,Martínek, Marek,Muchová, Lucie,Váňa, Ji?í,Vítek, Libor

, p. 3473 - 3489 (2020/03/25)

Carbon monoxide (CO) is a cell-signaling molecule (gasotransmitter) produced endogenously by oxidative catabolism of heme, and the understanding of its spatial and temporal sensing at the cellular level is still an open challenge. Synthesis, optical properties, and study of the sensing mechanism of Nile red Pd-based CO chemosensors, structurally modified by core and bridge substituents, in methanol and aqueous solutions are reported in this work. The sensing fluorescence "off-on" response of palladacycle-based sensors possessing low-background fluorescence arises from their reaction with CO to release the corresponding highly fluorescent Nile red derivatives in the final step. Our mechanistic study showed that electron-withdrawing and electron-donating core substituents affect the rate-determining step of the reaction. More importantly, the substituents were found to have a substantial effect on the Nile red sensor fluorescence quantum yields, hereby defining the sensing detection limit. The highest overall fluorescence and sensing rate enhancements were found for a 2-hydroxy palladacycle derivative, which was used in subsequent biological studies on mouse hepatoma cells as it easily crosses the cell membrane and qualitatively traces the localization of CO within the intracellular compartment with the linear quantitative response to increasing CO concentrations.

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