51548-88-0

Basic information

• Product Name: 1,2:4,5-BIS-O-(1-METHYLETHYLIDENE)-MUCO-INOSITOL
• Synonyms: 1,2:4,5-BIS-O-(1-METHYLETHYLIDENE)-MUCO-INOSITOL
• CAS NO: 51548-88-0
• Molecular Formula: C₁₂H₂₀O₆
• Molecular Weight: 260.28
• Mol File: 51548-88-0.mol
• Article Data: 15

Chemical Properties

• Melting Point: 184 °C(Solv: benzene (71-43-2))
• Boiling Point: 435.7±45.0 °C(Predicted)
• Appearance: /
• Density: 1.240±0.06 g/cm3(Predicted)
• PKA: 12.68±0.70(Predicted)
• CAS DataBase Reference: 1,2:4,5-BIS-O-(1-METHYLETHYLIDENE)-MUCO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2:4,5-BIS-O-(1-METHYLETHYLIDENE)-MUCO-INOSITOL(51548-88-0)
• EPA Substance Registry System: 1,2:4,5-BIS-O-(1-METHYLETHYLIDENE)-MUCO-INOSITOL(51548-88-0)

Safety Data

• Hazardous Substances Data: 51548-88-0(Hazardous Substances Data)

Usage

Chemical Family

Inositol family

Industry Applications

Pharmaceutical and food industries

Derivative of

Inositol

Structural Modification

Addition of two methyl ethylidene groups to the 1 and 5 positions of the inositol molecule

Pharmacological Properties

Potential antioxidant and ability to improve insulin sensitivity

Potential Use

Sweetener in food products due to sugar-like properties

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

• 129094-34-4 Benzoic acid (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 
• 87-89-8 D-myo-inositol 
• 38876-99-2 1L-chiro-inositol 
• 643-10-7 allo-inositol 
• 602278-90-0 D-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-isopropylidene-myo-inositol 
• 602278-89-7 L-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-isopropylidene-myo-inositol 
• 131146-87-7 (±)-1-O-allyl-4-O-benzyl-2,3:5,6-di-O-isopropylidene-myo-inositol 
• 111392-25-7 (+/-)-1,2:4,5-di-O-isopropylidene-6-O-p-methoxybenzyl-myo-inositol 
• 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 

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.