23095-14-9 Usage
General Description
4-Bromo-2-(aminosulphonyl)anisole is a chemical compound with the formula C7H8BrNO3S. It is an aromatic compound that contains a bromine atom, an amino group, and a sulphonyl group attached to a methoxy group. 4-BROMO-2-(AMINOSULPHONYL)ANISOLE is used in organic synthesis and as a building block for the production of pharmaceuticals and other specialty chemicals. It has potential applications in the pharmaceutical industry as a precursor for the synthesis of various drugs and active pharmaceutical ingredients. Furthermore, it has also been studied for its potential use in the development of new materials and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 23095-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,9 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23095-14:
(7*2)+(6*3)+(5*0)+(4*9)+(3*5)+(2*1)+(1*4)=89
89 % 10 = 9
So 23095-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BrNO3S/c1-12-6-3-2-5(8)4-7(6)13(9,10)11/h2-4H,1H3,(H2,9,10,11)
23095-14-9Relevant articles and documents
Design of Benzoxathiazin-3-one 1,1-Dioxides as a New Class of Irreversible Serine Hydrolase Inhibitors: Discovery of a Uniquely Selective PNPLA4 Inhibitor
Kornahrens, Anne F.,Cognetta, Armand B.,Brody, Daniel M.,Matthews, Megan L.,Cravatt, Benjamin F.,Boger, Dale L.
supporting information, p. 7052 - 7061 (2017/05/31)
The design and examination of 4,1,2-benzoxathiazin-3-one 1,1-dioxides as candidate serine hydrolase inhibitors are disclosed, and represent the synthesis and study of a previously unexplored heterocycle. This new class of activated cyclic carbamates provi
Novel N-dealkylation of N-alkyl sulfonamides and N,N-dialkyl sulfonamides with periodic acid catalyzed by chromium(III) acetate hydroxide
Xu, Liang,Zhang, Suhong,Trudell, Mark L.
, p. 1901 - 1904 (2007/10/03)
Chromium(III) acetate hydroxide has been found to be an efficient catalyst for N-dealkylation of N-alkyl sulfonamides and N,N-dialkyl sulfonamides to furnish sulfonamides in good to excellent yields with periodic acid in acetonitrile at room temperature.
