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2H-1,2,3,4-Benzothiatriazine, 2-(4-methoxyphenyl)-, 1,1-dioxide, also known as methoxybenthiazide, is a heterocyclic compound belonging to the benzothiatriazine class. It is a derivative of benzothiadiazine and is recognized for its pharmaceutical applications, particularly as an antihypertensive agent.
Used in Pharmaceutical Industry:
2H-1,2,3,4-Benzothiatriazine, 2-(4-methoxyphenyl)-, 1,1-dioxide is used as an antihypertensive agent for its ability to reduce blood pressure and enhance diuresis. It functions by inhibiting sodium reabsorption in the distal convoluted tubules of the kidneys, which leads to increased excretion of sodium and water.
Additionally, it is used as a potential anti-inflammatory and antioxidant agent due to its discovered properties that could contribute to various medical applications in the pharmaceutical industry.

65645-76-3

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65645-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65645-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,4 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65645-76:
(7*6)+(6*5)+(5*6)+(4*4)+(3*5)+(2*7)+(1*6)=153
153 % 10 = 3
So 65645-76-3 is a valid CAS Registry Number.

65645-76-3Downstream Products

65645-76-3Relevant academic research and scientific papers

One-pot synthesis ofN-substituted benzannulated triazolesviastable arene diazonium salts

Faggyas, Réka J.,McGrory, Rochelle,Sutherland, Andrew

, p. 6127 - 6140 (2021/07/21)

A mild and effective one-pot synthesis of 1,2,3-benzotriazin-4(3H)-ones and benzothiatriazine-1,1(2H)-dioxide analogues has been developed. The method involves the diazotisation and subsequent cyclisation of 2-aminobenzamides and 2-aminobenzenesulfonamidesviastable diazonium salts, prepared using a polymer-supported nitrite reagent andp-tosic acid. The transformation was compatible with a wide range of aryl functional groups and amide/sulfonamide-substituents and was used for the synthesis of pharmaceutically important targets. The synthetic utility of the one-pot diazotisaton-cyclisation process was further demonstrated with the preparation of an α-amino acid containing 1,2,3-benzotriazin-4(3H)-one.

Transition-Metal-Free Tandem Cyclization/ N-Arylation Reaction: A Method to Access Biaryl Sultam Derivatives via a Diradical Pathway

Thorat, Vijaykumar H.,Hsieh, Jen-Chieh,Cheng, Chien-Hong

supporting information, p. 6623 - 6627 (2020/09/02)

A novel procedure for the transition-metal-free tandem cyclization/N-arylation reaction sequence of an aryne with a 1,2,3,4-benzothiatriazine-1,1-dioxide is reported. This reaction goes through the intramolecular homolytic cyclization to generate an N-H b

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