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N-n-butyl-4-hydroxy-1,8-naphthalenedicarboxylic anhydride is a complex organic compound with the chemical formula C18H18O5. It is derived from 1,8-naphthalenedicarboxylic anhydride, a dicarboxylic anhydride with a naphthalene core, by substituting one of the hydrogen atoms on the naphthalene ring with a butyl group and introducing a hydroxyl group at the 4-position. N-n-butyl-4-hydroxy-1,8-naphthalenedicarboxylic anhydride is known for its potential applications in the synthesis of various polymers and pharmaceuticals, particularly as a monomer in the production of polyamides and polyesters. Its anhydride structure allows for the formation of ester linkages, which are crucial in creating the backbone of these polymers. The compound's specific structure and properties make it a valuable intermediate in the chemical industry, contributing to the development of materials with diverse applications, from textiles to specialty coatings.

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791-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791-80-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 791-80:
(5*7)+(4*9)+(3*1)+(2*8)+(1*0)=90
90 % 10 = 0
So 791-80-0 is a valid CAS Registry Number.

791-80-0Upstream product

791-80-0Relevant academic research and scientific papers

A two-photon fluorescent probe for colorimetric and ratiometric monitoring of mercury in live cells and tissues

Chen, Liyan,Park, Sang Jun,Wu, Di,Kim, Hwan Myung,Yoon, Juyoung

, p. 1766 - 1769 (2019)

Owing to the extreme toxicity of mercury, methods for its selective and sensitive sensing in solutions, and in live cells and tissues are in great demand. In this study, we developed a naphthalimide-based diphenylphosphinothioyl group-containing fluorescent and colorimetric probe that selectively detects mercury (Hg2+). Upon addition of mercury (Hg2+) to a solution of the probe, both a colorimetric change from colorless to yellow and a fluorescence change from blue to green (under a 365 nm hand-held UV lamp) occur, both of which can be observed using the "naked-eye". Furthermore, the probe possesses the capability of sensing intracellular mercury in both live cells and tissues using dual-emission channels and two-photon microscopy.

Mechanochemical activation of disulfide-based multifunctional polymers for theranostic drug release

Shi, Zhiyuan,Song, Qingchuan,G?stl, Robert,Herrmann, Andreas

, p. 1668 - 1674 (2021/02/22)

Drug delivery systems responsive to physicochemical stimuli allow spatiotemporal control over drug activity to overcome limitations of systemic drug administration. Alongside, the non-invasive real-time tracking of drug release and uptake remains challenging as pharmacophore and reporter function are rarely unified within one molecule. Here, we present an ultrasound-responsive release system based on the mechanochemically induced 5-exo-trigcyclization upon scission of disulfides bearing cargo molecules attachedviaβ-carbonate linker within the center of a water soluble polymer. In this bifunctional theranostic approach, we release one reporter molecule per drug molecule to quantitatively track drug release and distribution within the cell in real-time. We useN-butyl-4-hydroxy-1,8-naphthalimide and umbelliferone as fluorescent reporter molecules to accompany the release of camptothecin and gemcitabine as clinically employed anticancer agents. The generality of this approach paves the way for the theranostic release of a variety of probes and drugs by ultrasound.

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