62035-67-0 Usage
Uses
Used in Pharmaceutical Industry:
N-(3,4-dimethoxyphenyl)benzenesulfonamide is used as a therapeutic agent for its anti-inflammatory properties, making it a potential candidate for the treatment of conditions like rheumatoid arthritis. Its anti-cancer properties also position it as a potential agent in oncology for combating various types of cancer.
Used in Chemical Research:
In the field of chemical research, N-(3,4-dimethoxyphenyl)benzenesulfonamide is utilized as a building block in the synthesis of new pharmaceutical compounds, contributing to the development of innovative treatments and therapies.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, N-(3,4-dimethoxyphenyl)benzenesulfonamide is employed as an agent in the fight against microbial infections, potentially serving as an alternative or adjunct to existing antimicrobial treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 62035-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,3 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62035-67:
(7*6)+(6*2)+(5*0)+(4*3)+(3*5)+(2*6)+(1*7)=100
100 % 10 = 0
So 62035-67-0 is a valid CAS Registry Number.
62035-67-0Relevant academic research and scientific papers
Synthesis and biological evaluation of new disubstituted analogues of 6-methoxy-3-(3′,4′,5′-trimethoxybenzoyl)-1H-indole (BPR0L075), as potential antivascular agents
Ty, Nancy,Dupeyre, Gregory,Chabot, Guy G.,Seguin, Johanne,Tillequin, Francois,Scherman, Daniel,Michel, Sylvie,Cachet, Xavier
, p. 7494 - 7503 (2008/12/23)
6-Methoxy-3-(3′,4′,5′-trimethoxybenzoyl)-1H-indole (BPR0L075) (1) is a potent inhibitor of tubulin polymerization which exhibits both in vitro and in vivo activities against a broad spectrum of solid tumors. This compound was designed as a heterocyclic an
Cycloaddition reactions of 1,4-benzoquinone mono- And bisimides with styrenyl systems: New syntheses of nitrogen substituted azapterocarpans, pterocarpans, 2-aryl-2,3-dihydroindoles and -dihydrobenzofurans
Engler, Thomas A.
, p. 2713 - 2716 (2007/10/02)
Lewis acid-promoted reactions of 1,4-benzoquinones and 1,4-benzoquinone bis- and monoimides with various 2H-chromenes, N-tosyl-1,2-dihydroquinolines and styrenes regio- and stereoselectively produce the title compounds in good yields.
