(S)-(2,2-dimethyl-1,3-dioxolan-4-yl)methanol

(S)-(2,2-Dimethyl-1,3-dioxolan-4-yl)methanol serves as a key chiral building block for MEK inhibitors with antitumor activity and phospholipid synthesis. This protected glyceraldehyde derivative undergoes stereospecific reactions including ring-opening and esterification to construct essential chiral intermediates for both anticancer therapeutics and phosphoglyceride derivatives, enabling precise molecular assembly in pharmaceutical development.

Synonyms: 1,3-Dioxolane-4-methanol, 2,2-dimethyl-, (S)-;(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol,98%;(4S)-(+)-2,2-Dimethyl-4-(hydroxymethyl)-1,3-dioxolane 98%;(S)-(+)-1,2-Isopropylideneglycerol, [(4S)-(+)-2,2-Dimethyl-1,3-dioxolan-4-yl]methanol, (S)-Solketal;(S)-(+)-2,2-DiMethyl-1,3-Dioxalane-4-Methanol;(S)-(+)-2,2-DiMethyl-1,3-dioxolane-4-Methanol, 98% 5GR;D-1,2-O-ISOPROPYLIDENE-SN-GLYCEROL;D-(+)-1,2-ISOPROPYLIDENEGLYCEROL

EINECS: 244-910-8

Product Categories: Miscellaneous;Inhibitors;pharmacetical;Chiral Reagent;Chiral Reagents;Chiral Building Blocks;Dioxanes & Dioxolanes;Dioxolanes;Glycidyl Compounds, etc. (Chiral);Synthetic Organic Chemistry;Heterocycles

Mol File: 22323-82-6.mol