104340-86-5 Usage
Uses
Used in Gastrointestinal Medicine:
Leminoprazole is used as a therapeutic agent for the treatment of acid-related disorders, such as gastroesophageal reflux disease, peptic ulcers, and Zollinger-Ellison syndrome. Its rapid onset of action and well-tolerated nature provide relief for patients experiencing gastrointestinal symptoms.
Used in Pharmaceutical Industry:
Leminoprazole is utilized as an active pharmaceutical ingredient in the development of medications aimed at managing acid-related disorders. Its improved efficacy and tolerability compared to traditional proton pump inhibitors make it a valuable addition to the pharmaceutical market, offering patients a more effective and safer treatment option.
Check Digit Verification of cas no
The CAS Registry Mumber 104340-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,4 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104340-86:
(8*1)+(7*0)+(6*4)+(5*3)+(4*4)+(3*0)+(2*8)+(1*6)=85
85 % 10 = 5
So 104340-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H23N3OS/c1-14(2)12-22(3)18-11-7-4-8-15(18)13-24(23)19-20-16-9-5-6-10-17(16)21-19/h4-11,14H,12-13H2,1-3H3,(H,20,21)
104340-86-5Relevant academic research and scientific papers
PROCESS FOR SYNTHESIS OF SUBSTITUTED SULPHOXIDES
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, (2008/06/13)
A novel process for enantioselective synthesis of single enantiomers of omeprazole or its alkaline salts, of other optically pure substituted 2-(2-pyridinylmethyl-sulphinyl) -1H-benzimidazoles as well as of other structurally related sulphoxides or their alkaline salts. The claimed process is an asymmetric oxidation of a pro-chiral sulphide to the single enantiomers or an enantiomerically enriched form of the corresponding sulphoxide. The application also claims the enantiomeric sulphoxide products produced by the process and their use in medicine
