62035-67-0 Usage
General Description
N-(3,4-dimethoxyphenyl)benzenesulfonamide is a chemical compound with the molecular formula C14H15NO4S. It is a sulfonamide derivative with a sulfonamide functional group attached to a benzene ring substituted with a 3,4-dimethoxyphenyl group. N-(3,4-dimethoxyphenyl)benzenesulfonamide has various biological and pharmacological activities, including anti-inflammatory, anti-cancer, and antimicrobial properties. It has been studied for its potential therapeutic applications in the treatment of various diseases, including cancer, rheumatoid arthritis, and microbial infections. Additionally, it has been investigated for its potential as a building block in the synthesis of new pharmaceutical compounds and as a tool in chemical research.
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 articles and documents
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
Reaction of propenylbenzene derivatives and their analogs. I. Reaction of N,N dibromobenzenesulfonamide with propenylbenzene derivatives
Adachi,Otsuki
, p. 2803 - 2809 (2007/10/12)
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