90694-04-5

Usage

Synonyms

After myo-inositol

Function

Protective group in organic synthesis

Purpose

Temporarily masks hydroxyl groups on myo-inositol

Application

Selective manipulation of specific hydroxyl groups

Use in synthesis

Synthesis of complex organic molecules

Additional uses

Preparation of lipids, phospholipids, and inositol derivatives

Physical state

White crystalline solid

Melting point

200-202°C

Solubility

Not readily soluble in water

Upstream product

• 116-11-0 2-Methoxypropene 
• 87-89-8 D-myo-inositol 

Downstream Products

• 488-58-4 epi-Inositol 
• 38643-30-0 (+/-)-O¹,O²;O³,O⁴-diisopropylidene-epi-inositol 
• 52079-86-4 (1R)-(+)-(1,2,3/4,5)-2,3,4,5-tetrahydroxycyclohexane-1-methanol penta-acetate 
• 52079-85-3 (1R)-(+)-(1,2,3/4,5)-2,3,4,5-tetrahydroxycyclohexane-1-methanol 
• 90626-78-1 1L-(1,2,3,5/4)-5-(2-Acetoxymethyl-1,3-dithian-2-yl)-1-O-acetyl-4-O-benzyl-2,3-O-isopropyliden-1,2,3,4-cyclohexantetrol 
• 90626-79-2 2L-(2,3,5/4)-4-O-Benzyl-5-(2-ethoxycarbonyl-1,3-dithian-2-yl)-2,3-O-isopropyliden-2,3,4-trihydroxycyclohexanon 
• 90626-66-7 1L-4-O-Benzyl-3-desoxy-1,2:5,6-di-O-isopropyliden-3-C-<(2-methoxyethoxy)methoxymethyl>-allo-inosit 
• 90626-84-9 Acetic acid (3aR,4R,6S,7R,7aS)-6-(2-acetoxy-acetyl)-7-benzyloxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-yl ester 
• 90626-82-7 1L-(1,2,3,5/4)-5-Acetoxymethyl-1-O-acetyl-4-O-benzyl-2,3-O-isopropyliden-1,2,3,4-cyclohexantetrol 
• 90626-62-3 1L-3-O-Acetyl-4-O-benzyl-1,2:5,6-di-O-isopropyliden-chiro-inosit 
• 90652-13-4 1L-3-C-Acetoxymethyl-4-O-benzyl-3-desoxy-1,2:5,6-di-O-isopropyliden-allo-inosit 
• 90626-70-3 2D-(2,3,6/4,5)-6-O-Benzyl-2,3:4,5-di-O-isopropyliden-1-methoxymethylen-2,3,4,5,6-cyclohexanpentol 
• 90626-83-8 (3aR,4R,6S,7R,7aS)-7-Benzyloxy-6-(2-hydroxymethyl-[1,3]dithian-2-yl)-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 90626-64-5 2D-(2,3,6/4,5)-6-O-Benzyl-2,3:4,5-di-O-isopropyliden-2,3,4,5,6-pentahydroxycyclohexanon 

Relevant academic research and scientific papers

Improved preparation of acetals of myo-inositol and its (+/-)-1-benzyl ether: conformational analysis of di-O-isopropylidene-myo-inositol derivatives

The acid-catalysed reactions of myo-inositol with 3-5 equiv. of 2-methoxypropene or 2,2-dimethoxypropane in methyl sulfoxide or N,N-dimethylformamide gave mixtures of the 1,2:4,5-, 1,2:5,6-, and 1,2:3,4-di-O-isopropylidene derivatives with little or none