75348-12-8

Basic information

• Product Name: 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-chiro-inositol
• Synonyms: 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-chiro-inositol
• CAS NO: 75348-12-8
• Molecular Weight: 480.558
• Mol File: 75348-12-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-chiro-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-chiro-inositol(75348-12-8)
• EPA Substance Registry System: 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-chiro-inositol(75348-12-8)

Safety Data

• Hazardous Substances Data: 75348-12-8(Hazardous Substances Data)

Upstream product

• 80970-96-3 1L-1-C-Hydroxymethyl-1,7:2,3:5,6-tri-O-isopropyliden-chiro-inosit 
• 75348-10-6 1L-1-C-Hydroxymethyl-3,4:5,6-di-O-isopropyliden-2-O-methyl-chiro-inosit 
• 75251-60-4 1L-1,7-Anhydro-1-C-hydroxymethyl-3,4:5,6-di-O-isopropyliden-2-O-methyl-chiro-inosit 
• 75420-23-4 1L-1-C-Hydroxymethyl-1,7:5,6-di-O-isopropyliden-chiro-inosit 
• 29070-89-1 1L-1-C-Hydroxymethyl-chiro-inosit 
• 80970-98-5 1L-4-O-Benzyl-1-C-hydroxymethyl-1,7:2,3:5,6-tri-O-isopropyliden-chiro-inosit 
• 80970-99-6 1L-4-O-Benzyl-1-C-hydroxymethyl-1,7:5,6-di-O-isopropyliden-chiro-inosit 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 75348-11-7 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-1,7:5,6-di-O-isopropyliden-chiro-inosit 

Downstream Products

• 81713-11-3 (1R,4R,5S,6S)-3-Aminomethyl-4,5,6-tris-benzyloxy-cyclohex-2-enylamine 
• 81713-05-5 2L-(2,3,5/4,6)-4,5,6-Tri-O-benzyl-1-C-methylen-2-O-methylsulfonyl-3-O-p-tolylsulfonylpentahydroxycyclohexan 
• 81712-82-5 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-5,6-O-isopropyliden-7-O-p-tolylsulfonyl-chiro-inositol 
• 81713-03-3 2L-(2,3,5/4,6)-4,5,6-Tri-O-benzyl-1-C-methylen-3-O-p-tolylsulfonyl-chiro-inositol 
• 81712-80-3 1L-7-O-Benzoyl-2,3,4-tri-O-benzyl-1-C-hydroxymethyl-5,6-O-isopropyliden-chiro-inositol 
• 81713-01-1 1L-1,7-Anhydro-2,3,4-tri-O-benzyl-1-C-hydroxymethyl-5-O-p-tolylsulfonyl-chiro-inositol 
• 81726-68-3 Benzoic acid (1S,2R,3S,4R,6R)-2,3,4-triacetoxy-6-methanesulfonyloxy-5-methylene-cyclohexyl ester 
• 81712-81-4 1L-2,3,4-Tri-O-benzyl-1-C-hydroxymethyl-5,6-O-isopropyliden-chiro-inositol 
• 81712-88-1 2L-(2,3,5/4,6)-4,5,6-Tri-O-acetyl-3-O-benzoyl-1-C-methylenpentahydroxycyclohexane 
• 81739-83-5 7-Aminovalienamin 
• 81712-91-6 1L-(1,3/2,4)-5-C-Aminomethyltetrahydoxycyclohex-5-enydrochlorid 
• 81712-83-6 1L-1-C-Hydroxymethyl-5,6-O-isopropyliden-7-O-p-tolylsulfonyl-chiro-inositol 
• 81712-87-0 2L-(2,3,5/4,6)-4,5,6-Tri-O-acetyl-1-C-methylenpentahydroxycyclohexane 
• 75348-18-4 1L-(1,3/2,4)-Di-O-acetyl-2,3,4-tri-O-benzyl-5-C-hydroxymethyl-tetrahydroxy-5-cyclohexen 

Relevant articles and documents

Cyclitol Reactions, V. - Synthesis of Enantiomerically Pure Valienamine from Quebrachitol

An enantioselective synthesis of Valienamine (86) from quebrachitol (L-2O-methyl-chiro-inositol) (1) is described.Valienamine (86) is an unsaturated branched-chain aminocyclitol found in the central structural unit of the antidiabetic drug acarbose.Techniques for the introduction of side chains, azido groups, and double bonds into inositol systems are investigated.The methods developed in this connection are applied in the synthesis of valienamine.