129094-34-4

Basic information

• Product Name: 1-O-BENZOYL-2,3:5,6-DI-O-ISOPROPYLIDENE-MYO-INOSITOL
• Synonyms: 1-O-BENZOYL-2,3:5,6-DI-O-ISOPROPYLIDENE-MYO-INOSITOL;1,2:4,5-Bis-O-(1-methylethylidene)-DL-chiro-inositol 6-benzoate
• CAS NO: 129094-34-4
• Molecular Formula: C₁₉H₂₄O₇
• Molecular Weight: 430.538
• Mol File: 129094-34-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-O-BENZOYL-2,3:5,6-DI-O-ISOPROPYLIDENE-MYO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-BENZOYL-2,3:5,6-DI-O-ISOPROPYLIDENE-MYO-INOSITOL(129094-34-4)
• EPA Substance Registry System: 1-O-BENZOYL-2,3:5,6-DI-O-ISOPROPYLIDENE-MYO-INOSITOL(129094-34-4)

Safety Data

• Hazardous Substances Data: 129094-34-4(Hazardous Substances Data)

Usage

Derived from

myo-inositol

Usage

commonly used in the synthesis of various pharmaceuticals and biologically active compounds

Role in organic chemistry

a versatile building block, used for the preparation of carbohydrate-derived structures and as a chiral auxiliary in asymmetric synthesis

Therapeutic applications

studied for potential use in the treatment of metabolic disorders and diabetes

Other potential uses

shown promise as an anti-inflammatory agent and has been investigated for its potential in cancer therapy.

Upstream product

• 129094-33-3 1,2:4,5-Di-O-isopropylidene-myo-inositol monotriflate 
• 553-54-8 lithium benzoate 
• 128110-25-8 (L)-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 10364-94-0 1-benzoylimidazole 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 

Downstream Products

• 58706-24-4 (+/-)-6-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131146-88-8 (±)-1-O-allyl-4-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 131146-97-9 (1R,2S,3S,4R,5R,6S)-3,4,5-Tris-allyloxy-6-benzyloxy-cyclohexane-1,2-diol 
• 131146-87-7 (±)-1-O-allyl-4-O-benzyl-2,3:5,6-di-O-isopropylidene-myo-inositol 
• 131146-96-8 (±)-2,3-O-isopropylidene-1,5,6-tri-O-allyl-4-O-benzyl-myo-inositol 
• 135182-39-7 (1S,2R,3S,4R,5S,6S)-2,3,4-Tris-allyloxy-5-benzyloxy-6-methoxymethoxy-cyclohexanol 
• 135182-40-0 (1R,2R,3S,4R,5R,6R)-3,4,5-Tris-allyloxy-2,6-bis-benzyloxy-cyclohexanol 
• 135182-41-1 {3-[Benzyloxy-((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxy-3,4,5-trihydroxy-cyclohexyloxy)-phosphoryloxy]-propyl}-carbamic acid benzyl ester 

Relevant articles and documents

Affinity probes for ins(1,3,4,5)P4 receptors

A P-1-tethered derivative of Ins(1,3,4,5)P4 was synthesized and used to prepare a bioselective affinity matrix and a photoaffinity label for purification and covalent modification of IP4 receptor proteins.