247088-70-6

Basic information

• Product Name: L-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol
• Synonyms: L-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol
• CAS NO: 247088-70-6
• Molecular Weight: 678.968
• Mol File: 247088-70-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol(CAS DataBase Reference)
• NIST Chemistry Reference: L-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol(247088-70-6)
• EPA Substance Registry System: L-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol(247088-70-6)

Safety Data

• Hazardous Substances Data: 247088-70-6(Hazardous Substances Data)

Upstream product

• 51019-44-4 (S)-2-chloro-2-oxo-1-phenylethyl acetate 
• 678142-81-9 1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol 
• 7322-88-5 (S)-acetylmandelic acid 

Downstream Products

• 608880-29-1 C₇₃H₁₁₂O₁₈P₂ 
• 608880-30-4 Hexadecanoic acid (R)-2-{benzyloxy-[(1R,2S,3R,4R,5S,6R)-3-(bis-benzyloxy-phosphoryloxy)-2,5,6-trihydroxy-4-(4-oxo-pentanoyloxy)-cyclohexyloxy]-phosphoryloxy}-1-hexadecanoyloxymethyl-ethyl ester 
• 608880-23-5 5-dibenzyl L-1,2-O-cyclohexylidene-6-O-levulinoyl-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol phosphate 
• 608880-25-7 5-dibenzyl L-1,2-O-cyclohexylidene-6-O-levulinoyl-myo-inositol phosphate 
• 848574-00-5 C₄₈H₆₇O₁₂PSi₂ 

Relevant articles and documents

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 natural PI(3,4,5)P3

Natural phosphatidylinositol 3,4,5-trisphosphate which has been believed to have stearoyl and arachidonoyl groups at the sn-1 and -2 positions, respectively, has been synthesized using 1,2-O-cyclohexylidene 3,4-O-disiloxanyl-myo-inositol as the pivotal intermediate.