754197-60-9

Upstream product

• 6848-53-9 L-3,4:5.6-di-O-cyclohexylidene-2-O-methyl-(-)-chiro-inositol 
• 754197-57-4 1L-1,2-O-cyclohexylidene-5-O-methyl-chiro-inositol 
• 754197-58-5 C₁₆H₂₈O₆ 
• 17230-42-1 3,4,5,6-Tetra-O-methyl-(-)-inosit; L-(1,2,4-3,5,6)-3,4,5,6-Tetramethoxy-1,2-cyclohexandiol 
• 642-38-6 quebrachitol 
• 754197-59-6 (1R,2R,3R,4S,5R,6R)-2-Benzyloxy-3,4,5,6-tetramethoxy-cyclohexanol 
• 100-39-0 benzyl bromide 

Downstream Products

• 117708-51-7 ((1R,2S,3S,4R,5S,6R)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene 
• 754197-62-1 (1S,2R,3R,4S,5R,6R)-2-Benzyloxy-3,4,5,6-tetramethoxy-cyclohexanol 

Relevant academic research and scientific papers

Enzyme-catalysed synthesis of galactosylated 1D- and 1L-chiro-inositol, 1D-pinitol, myo-inositol and selected derivatives using the β-galactosidase from the thermophile Thermoanaerobacter sp. strain TP6-B1

The products from the enzymatic β-D-galactopyranosylation of 1D-chiro-inositol, 1D-pinitol, 1D-3-O-allyl-4-O-methyl-chiro-inositol, 1D-3,4-di-O-methyl-chiro-inositol, 1L-chiro-inositol and myo-inositol in combined yields ranging from 46% to 64% have been