Alcohols

The (3R,4R)-Pyrrolidine-3,4-diol is a chiral compound that has a hydroxy group, a reactive carbonyl group, and a stereospecific carbonyl group. It is synthesized from the reaction of formaldehyde with aniline and hydrochloric acid. This chemical reacts with hydrogen in the presence of nickel catalyst to form (3S,4S)-pyrrolidine-3,4-diol. The enzyme binding of this compound has been shown to be stereoselective because it binds better to one type of enzyme than another. The kinetic studies have shown that the transfer of this compound is stereospecific because it reacts more readily with one type of enzyme than another.

Please enquire for more information about 4-(4'-Methoxyphenyl)-1-butanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-Methyl-1H-indazol-7-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Pyrrolidinol is a chemical compound that belongs to the group of organic compounds with the formula CHNO. It is a colorless liquid that can be prepared by oxidation of 3-hydroxypyridine with hydrogen sulfate. 3-Pyrrolidinol has been used as a cross-linker in biochemistry and as an experimental model protein in studies on enzymatic reactions. It has been shown to react with malic acid, which leads to the formation of 3-pyrrolidinol malonate, a model for the reaction between malonic acid and alcohols. The reaction proceeds via a reversible addition-elimination mechanism and is catalyzed by NAD+/NADH coenzyme system. 3-Pyrrolidinol has also been shown to have anticancer effects against HL60 cells in vitro and may have some potential as an anti-inflammatory agent for cancer treatment.

Please enquire for more information about (3R,5S)-5-(Hydroxymethyl)pyrrolidin-3-ol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Timolol is a beta-adrenergic blocker drug that is used to treat glaucoma and other eye diseases. Timolol blocks the action of catecholamines (e.g., adrenaline) on the beta-receptors in the eye, which decreases intraocular pressure. Timolol maleate is available as an ophthalmic solution and tablet for oral use. The most common side effect of timolol is constipation; however, it has been shown to cause bowel disease in some cases. Timolol also has been shown to have mitochondrial functions, inhibiting electron transport, and can have interactions with drugs such as benzalkonium chloride. The pharmacological effects of timolols are dose-dependent and reversible if discontinued. Timolols have been used in combination therapy groups for the treatment of intraocular hypertension or chronic open angle glaucoma in patients who are not responsive to conventional therapy with beta blockers or alpha agonists alone.

Please enquire for more information about 4-Ethyl-5-(3-methylphenyl)-4H-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Dimethylamine reacts with phosphotungstic acid to form a phosphotungstic chloride. This reaction has an optimal reaction time of 24 hours and is carried out in an organic solvent. The product, 6,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride hydrate, is synthesized by reacting the amine with a formylating agent such as oxalyl chloride or methyl chloroformate. The enantiomeric purity can be determined by analyzing the reaction solution using a chiral HPLC column.

Please enquire for more information about [(3S,4R)-4-(4-Chloro-2-fluorophenyl)pyrrolidin-3-yl]methanol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-(Aminomethyl)-1-methyl-3,4-dihydroquinolin-2(1H)-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page