2,3-O-Isopropylidene-D-ribonolactone is a nucleoside analogue that serves as an acetonide derivative of D-ribonolactone. It is primarily utilized as an intermediate in organic synthesis, formed through the acid-catalyzed acetalization of D-ribonolactone with acetone. This compound plays a critical role in the production of 1,5-dideoxy-1,5-imino-D-ribitol and 1,5-dideoxy-1,5-imino-L-arabinitol, making it valuable for various biochemical applications and research endeavors.
2,3-O-Isopropylidene-D-ribonolactone is a nucleoside analogue that serves as an acetonide derivative of D-ribonolactone. It is primarily utilized as an intermediate in organic synthesis, formed through the acid-catalyzed acetalization of D-ribonolactone with acetone. This compound plays a critical role in the production of 1,5-dideoxy-1,5-imino-D-ribitol and 1,5-dideoxy-1,5-imino-L-arabinitol, making it valuable for various biochemical applications and research endeavors.
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