98974-89-1

Basic information

• Product Name: 1.2:4,5-DI-O-ISOPROPYLIDENE-MYO-INOSITOL
• Synonyms: 1.2:4,5-DI-O-ISOPROPYLIDENE-MYO-INOSITOL;2,3:5,6-DI-O-(1-METHYLETHYLIDENE)-MYO-INOSITOL;IPRY2-INO;1,2:4,5-Bis-O-(1-Methylethylidene)- DL-Myo-inositol;1,2:4,5-Bis-O-(1-Methylethylidene)-Myo-inositol
• CAS NO: 98974-89-1
• Molecular Formula: C₁₂H₂₀O₆
• Molecular Weight: 260.284
• Product Categories: Inositols;Carbohydrates & Derivatives
• Mol File: 98974-89-1.mol
• Article Data: 15

Chemical Properties

• Melting Point: 172-174°C
• Appearance: /
• CAS DataBase Reference: 1.2:4,5-DI-O-ISOPROPYLIDENE-MYO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1.2:4,5-DI-O-ISOPROPYLIDENE-MYO-INOSITOL(98974-89-1)
• EPA Substance Registry System: 1.2:4,5-DI-O-ISOPROPYLIDENE-MYO-INOSITOL(98974-89-1)

Safety Data

• Hazardous Substances Data: 98974-89-1(Hazardous Substances Data)

Usage

Chemical Properties

White Crystalline Solid

Uses

Different sources of media describe the Uses of 98974-89-1 differently. You can refer to the following data:
1. 1,2:4,5-Diisopropylidene D,L-myo-Inositol is used in the synthesis of (±)-3-O-alkylated myo-inositol 1,4,5-trisphosphate analogs as potent receptor ligands and enzyme inhibitors.
2. 1,2:4,5-Diisopropylidene D,L-myo-Inositol is used in the synthesis of (-)-3-O-alkylated myo-inositol 1,4,5-trisphosphate analogs as potent receptor ligands and enzyme inhibitors.

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 67-64-1 acetone 
• 99756-37-3 (±)-3,6-di-O-benzoyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 116-11-0 2-Methoxypropene 

Downstream Products

• 191488-25-2 D-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 603126-53-0 1D-1,4-di-O-[(S)-O-acetylmandeloyl]-2,3:5,6-di-O-isopropylidene-myo-inositol 
• 161104-98-9 1-O-n-hexadecylphoryl-D-myo-inositol 
• 161105-02-8 Phosphoric acid hexadecyl ester (3aR,4S,4aR,7aS,8S,8aR)-8-hydroxy-2,2,6,6-tetramethyl-hexahydro-benzo[1,2-d;4,5-d']bis[1,3]dioxol-4-yl ester phenyl ester 
• 1391099-60-7 3-O-(4-bromobenzyl)-6-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-1,2:4,5-di-O-isopropylidene-D-myo-inositol 
• 1391725-13-5 3-O-(4-bromobenzyl)-6-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-1,2:4,5-di-O-isopropylidene-L-myo-inositol 
• 1391099-83-4 3-O-(4-bromobenzyl)-6-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-1,2-di-O-isopropylidene-D-myo-inositol 
• 1391099-61-8 3-O-(4-bromobenzyl)-4,5-di-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2-di-O-isopropylidene-D-myo-inositol 
• 131147-11-0 (±)-2,3-O-isopropylidene-1,5,6-tri-O-benzyl-4-O-allyl-myo-inositol 

Relevant articles and documents

A Chiral Phosphoramidite Reagent for the Synthesis of Inositol Phosphates

There is a paucity of chiral phosphoramidite reagents or chiral catalysis methods for the synthesis of biologically relevant inositol phosphates. A new C2-symmetrical chiral phosphoramidite has been developed and successfully applied to the syn

H2SO4-silica: An eco-friendly heterogeneous catalyst for the differential protection of myo-inositol hydroxyl groups

There is enormous interest in myo-inositol derivatives as they serve as precursors for the synthesis of several biologically important phosphoinositols, natural products, catalyst, supramolecular architectures etc. However the presence of six secondary hy

Stereoselective oxidation of protected inositol derivatives catalyzed by inositol dehydrogenase from Bacillus subtilis

Inositol dehydrogenase (EC 1.1.1.18) from Bacillus subtilis is shown to have a nonpolar cavity adjacent to the active site, allowing racemic protected inositol derivatives such as 4-O-benzyl-myo-inositol to be recognized with very high apparent stereoselectivity.