208191-64-4

Usage

Physical appearance

Yellow crystalline powder

Type of compound

Organic

Primary use

Pharmaceutical drug for antispasmodic properties

Specific application

Treatment of irritable bowel syndrome

Mechanism of action

Relaxes smooth muscles in the intestines

Benefits

Reduces abdominal pain and discomfort associated with gastrointestinal conditions

Safety

Considered safe and effective when used as directed

Possible side effects

Dizziness, headache, or nausea

Upstream product

• 38063-41-1 1-methoxy-2-(methylsulfonyl)-4-nitrobenzene 
• 2976-32-1 1-methanesulfonyl-3-nitro-benzene 
• 38452-13-0 1-methylsulfinyl-2-methoxybenzene 
• 2388-73-0 1-methoxy-2-(methylsulfanyl)benzene 
• 876497-01-7 2-methanesulfinyl-1-methoxy-4-nitro-benzene 
• 37407-27-5 2-(methylsulfanyl)-4-nitrophenol 

Downstream Products

• 1132942-72-3 2-iodo-6-(methylsulfonyl)-4-nitrophenol 
• 38063-41-1 1-methoxy-2-(methylsulfonyl)-4-nitrobenzene 

Relevant academic research and scientific papers

ANTI-INFECTIVE PYRIMIDINES AND USES THEREOF

This invention relates to: (a) compounds and salts thereof that, inter alia, inhibit HCV; (b) intermediates useful for the preparation of such compounds and salts; (c) compositions comprising such compounds and salts; (d) methods for preparing such intermediates, compounds, salts, and compositions; (e) methods of use of such compounds, salts, and compositions; and (f) kits comprising such compounds, salts, and compositions.

N-PHENYL-DIOXO-HYDROPYRIMIDINES USEFUL AS HEPATITIS C VIRUS (HCV) INHIBITORS

This invention relates to: (a) compounds and salts thereof that, inter alia, inhibit HCV; (b) intermediates useful for the preparation of such compounds and salts; (c) compositions comprising such compounds and salts; (d) methods for preparing such interm

Hydroxylation of Nitroarenes with Alkyl Hydroperoxide Anions via Vicarious Nucleophilic Substitution of Hydrogen

Rhone-Poulenc Polska Ltd., ul. Grzybowska 80/82, 00-844 Warszawa, Poland Garbo- and heterocyclic nitroarenes react with anions of tert-butyl and cumyl hydroperoxides in the presence of strong bases to form substituted o- and p-nitrophenols. The reaction usually proceeds in high yields and is of practical value as a method of synthesis and manufacturing of nitrophenols. Orientation of the hydroxylation can be controlled to a substantial extent by selection of the proper conditions. Basic mechanistic features of this process were clarified.