790272-26-3 Usage
Uses
Used in Pharmaceutical Industry:
(4-HYDROXYPHENYL)METHYL(2-NAPHTHYLSULFONYL)AMINE is utilized as an active pharmaceutical ingredient for the development of medications targeting various medical conditions. Its anti-inflammatory and analgesic properties make it a potential candidate for treating pain and inflammation-related disorders.
Used in Dye Production:
In the dye industry, (4-HYDROXYPHENYL)METHYL(2-NAPHTHYLSULFONYL)AMINE serves as a key compound in the creation of dyes. Its chemical structure contributes to the color-producing properties required for various applications, including textiles, plastics, and printing inks.
Used in Cardiovascular Disease Treatment:
(4-HYDROXYPHENYL)METHYL(2-NAPHTHYLSULFONYL)AMINE is being studied for its potential role in the treatment of cardiovascular diseases. Its specific properties may offer therapeutic benefits in managing or treating conditions related to the heart and circulatory system.
Used in Cancer Therapy:
(4-HYDROXYPHENYL)METHYL(2-NAPHTHYLSULFONYL)AMINE is also under investigation for its potential use in cancer treatment. Research is exploring how (4-HYDROXYPHENYL)METHYL(2-NAPHTHYLSULFONYL)AMINE may contribute to the development of new cancer therapies, possibly enhancing the effectiveness of existing treatments or providing new avenues for intervention against cancer cells.
Check Digit Verification of cas no
The CAS Registry Mumber 790272-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,2,7 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 790272-26:
(8*7)+(7*9)+(6*0)+(5*2)+(4*7)+(3*2)+(2*2)+(1*6)=173
173 % 10 = 3
So 790272-26-3 is a valid CAS Registry Number.
790272-26-3Relevant articles and documents
O- and N-substituted derivatives of planetol as valuable bioactive compounds
Irshad, Misbah,Abbasi, Muhammad Athar,Aziz-Ur-Rehman,Rasool, Shahid,Siddiqui, Sabahat Zahra,Ahmad, Irshad,Ashraf, Muhammad,Lodhi, Muhammad Arif,Jamal, Syed Babar
, p. 1151 - 1160 (2014/06/09)
The compounds bearing sulfamoyl and acetamoyl groups have been found to show various biological activities. In the present research work, a series of O- and N-substituted derivatives were synthesized, starting with planetol (1). First N-methyl-4-hydroxyanilinium sulfate (1; planetol or metol) was treated with different aryl sulfonyl chlorides (2a-i) using aq. sodium carbonate solution as reaction medium to yield N-substituted derivatives 3a-i. The electrophile, N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-bromoacetamide (5) was prepared by the reaction of 2,3-dihydro-1,4-benzodioxin-6-amine (4) and 2-bromoacetylbromide in a weak basic aqueous medium. The target O-substituted molecules 6a-i, were synthesized by gearing up the electrophile 5, with the molecules 3a-i, in a polar aprotic solvent using LiH as an activator. The proposed structures of all the synthesized molecules were corroborated by IR,1H NMR and EIMS spectral data. The in vitro enzyme inhibition and antibacterial studies rendered the synthesized molecules as better cholinesterase inhibitors and moderately better antibacterial agents. To explore the binding modes of the synthesized compounds, all of them were computationally docked against the active sites of acetyl cholinesterase (AChE), butyryl cholinesterase (BChE) and lipoxygenase (LOX). The compounds showed significant interactions and good correlation with the experimental data.
