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One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Safety of (R)-2-Oxothiazolidine-4-carboxylic acid, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 19771-63-2

The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. An article , which mentions Safety of (R)-2-Oxothiazolidine-4-carboxylic acid, molecular formula is C4H5NO3S. The compound – (R)-2-Oxothiazolidine-4-carboxylic acid played an important role in people’s production and life., Safety of (R)-2-Oxothiazolidine-4-carboxylic acid

Oxazolidin-2-ones and thiazolidin-2-ones are conveniently prepared by condensation of L-serine, L-threonine and L-cysteine, respectively with triphosgene. The corresponding methyl esters may be subsequently obtained by quenching the reaction mixture with methanol, without prior need for the isolation of the free acids. An improved procedure for preparation of triphosgene using an internal cooling system is described.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Safety of (R)-2-Oxothiazolidine-4-carboxylic acid, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 19771-63-2

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H662N | ChemSpider