678142-80-8

Basic information

• Product Name: D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol
• Synonyms: D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol
• CAS NO: 678142-80-8
• Molecular Weight: 678.968
• Mol File: 678142-80-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: D-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: D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol(678142-80-8)
• EPA Substance Registry System: D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol(678142-80-8)

Safety Data

• Hazardous Substances Data: 678142-80-8(Hazardous Substances Data)

Upstream product

• 51019-44-4 (S)-2-chloro-2-oxo-1-phenylethyl acetate 
• 7322-88-5 (S)-acetylmandelic acid 
• 204253-96-3 1D-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol 

Downstream Products

• 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 
• 204253-96-3 1D-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol 
• 55123-25-6 D-1,2-O-cyclohexylidene-myo-inositol 
• 608880-26-8 C₄₅H₅₂O₁₄P₂ 
• 608880-22-4 5-dibenzyl D-1,2-O-cyclohexylidene-6-O-levulinoyl-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol phosphate 
• 608880-27-9 D-6-O-levulinoyl-myo-inositol 3,5-bis(dibenzyl phosphate) 
• 608880-24-6 5-dibenzyl D-1,2-O-cyclohexylidene-6-O-levulinoyl-myo-inositol phosphate 
• 848574-01-6 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.