34361-60-9

Basic information

• Product Name: 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol
• CAS NO: 34361-60-9
• Molecular Weight: 340.417
• Mol File: 34361-60-9.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol(34361-60-9)
• EPA Substance Registry System: 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol(34361-60-9)

Safety Data

• Hazardous Substances Data: 34361-60-9(Hazardous Substances Data)

Upstream product

• 1122-84-5 1-ethoxycyclohexene 
• 6763-47-9 rac-1,2-O-cyclohexylidene-myo-inositol 
• 111901-83-8 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-D-myo-inositol 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-D-myo-inositol 
• 801301-07-5 L-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-cyclohexylidene-myo-inositol 
• 126647-64-1 2,3:5,6-(1,2:4,5)-dicyclohexylidene-myo-inositol 1,4-(3,6)-biscamphanate 
• 111828-85-4 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-L-myo-inositol 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-L-myo-inositol 
• 801301-08-6 D-3,6-di-O-[(S)-O-acetylmandeloyl]-1,2-O-cyclohexylidene-myo-inositol 
• 126647-64-1 2,3:5,6-(1,2:4,5)-dicyclohexylidene-myo-inositol 1,4-(3,6)-biscamphanate 
• 87-89-8 D-myo-inositol 
• 134109-13-0 D-3-O-benzoyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 129115-29-3 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-trifluoromethanesulfonyl-D-myo-inositol 
• 129094-32-2 1,2;4,5-Di-O-cyclohexylidene-3-O-trifluoromethanesulfonyl-myo-inositol 

Downstream Products

• 23486-92-2 1L(1D)-1,4(3,6)-di-O-benzyl-2,3:5,6(1,2:4,5)-di-O-cyclohexylidene-myo-inositol 
• 34361-60-9 D-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 34361-60-9 1L-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 26277-05-4 1,2,4,5,6-penta-O-benzyl-sn-myo-inositol 
• 131146-91-3 (+/-)-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 114218-29-0 1L-1-O-allyl-2,3,4,5,6-penta-O-benzyl-myo-inositol 
• 136282-32-1 6-O-allyl-3-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 134039-17-1 C₂₃H₃₂O₇ 
• 136282-38-7 1,4-di-O-allyl-5,6-di-O-benzyl-3-O-tert-butyldimethylsilyl-myo-inositol 
• 129879-49-8 6-O-allyl-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 
• 134039-19-3 (1R,2S,3S,4R,5R,6S)-3-Allyloxy-4,5-bis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 134039-16-0 C₂₉H₄₀O₇ 
• 136282-40-1 2,5,6-tri-O-benzyl-1,4-di-O-trans-prop-1-enyl-myo-inositol 
• 136282-33-2 4-O-allyl-1,5,6-tri-O-benzyl-3-O-tert-butyldimethylsilyl-myo-inositol 

Relevant articles and documents

GLYCOSYL-INOSITOL DERIVATIVES III. SYNTHESIS OF HEXOSAMINE-INOSITOL-PHOSPHATES RELATED TO PUTATIVE INSULIN MEDIATORS

The disaccharides related to glycosyl phosphatidyl inositol anchors of membrane proteins, 4-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-D-myo-inositol-1-phosphate and 4-O-(2-amino-2-deoxy-α-D-galactopyranosyl)-D-chiro-inositol-1-phosphate, have been prepared from optically resolved myo-inositol derivatives.The chiro-inositol moiety was obtained by epimerization of a selectively blocked myo-inositol-triflate ester.The resolved inositols were subsequently phosphorylated to yield the disaccharide aglycones.The amino-sugar components were prepared by azidonitration of suitably protected glucal and galactal derivatives.The derived pyranosyl chlorides were then condensed with the inositol phosphates using silver triflate as the promoter.

Resolution of synthetically useful myo-inositol derivatives using the chiral auxiliary O-acetylmandelic acid

Efficient methods for the resolution of various myo-inositol derivatives have been developed using O-acetylmandelic acid (OAM) as the chiral auxiliary. Various methods of introduction of the chiral auxiliary have been compared. DCC mediated coupling betwe

Synthesis of phosphatidylinositol mannosides (PIMs)

Two strategies towards the synthesis of phosphatidylinositol mannosides (PIMs) were elaborated which permit selective access to the O-1-, O-2-, and the O-6 position of the myo-inositol residue. Starting materials are 1,2:5,6- and 1,2:4,5-di-O-cyclohexylid