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4-phenoxy-N-butyl-1,8-naphthalimide is a chemical compound with the molecular formula C22H17NO3. It is a derivative of 1,8-naphthalimide, which is a heterocyclic aromatic compound consisting of a naphthalene ring fused to an imide group. The 4-phenoxy substituent in 4-phenoxy-N-butyl-1,8-naphthalimide is a phenol group attached to the naphthalene ring, while the N-butyl group is a four-carbon alkyl chain attached to the nitrogen atom of the imide group. 4-phenoxy-N-butyl-1,8-naphthalimide is often used as a fluorescent probe in various applications, such as in the detection of metal ions, pH sensing, and as a labeling agent in biochemistry. Its properties, such as high quantum yield and photostability, make it a valuable tool in scientific research and diagnostics.

2494-95-3

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2494-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2494-95-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2494-95:
(6*2)+(5*4)+(4*9)+(3*4)+(2*9)+(1*5)=103
103 % 10 = 3
So 2494-95-3 is a valid CAS Registry Number.

2494-95-3Downstream Products

2494-95-3Relevant academic research and scientific papers

Facile synthesis, sensor activity and logic behaviour of 4-aryloxy substituted 1,8-naphthalimide

Marinova, Nevena V.,Georgiev, Nikolai I.,Bojinov, Vladimir B.

, p. 54 - 61 (2013)

A series of 4-phenoxy- and 4-alkoxy-1,8-naphthalimide fluorophores have been synthesized in high yields at room temperature applying novel facile synthesis. One of the compounds was designed as a fluorescent PET sensor according to the fluorophore-spacer-receptor model. The ability of this molecule to detect protons and transition metal cations with pronounced selectivity towards Fe3+ was demonstrated. Moreover the 4-phenoxy substituted 1,8-naphthalimides were highly solvent sensitive and able to detect small quantities of water. The potential of the 1,8-naphthalimide sensor to execute INHIBIT logic function at molecular level was also demonstrated.

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