651313-77-8

Basic information

• Product Name: Phosphorous acid dibenzyl ester (1S,2S,3R,4R,5R,6S)-2,5-bis-benzyloxy-3,4,6-tris-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester
• CAS NO: 651313-77-8
• Molecular Weight: 1337.33
• Mol File: 651313-77-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phosphorous acid dibenzyl ester (1S,2S,3R,4R,5R,6S)-2,5-bis-benzyloxy-3,4,6-tris-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphorous acid dibenzyl ester (1S,2S,3R,4R,5R,6S)-2,5-bis-benzyloxy-3,4,6-tris-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester(651313-77-8)
• EPA Substance Registry System: Phosphorous acid dibenzyl ester (1S,2S,3R,4R,5R,6S)-2,5-bis-benzyloxy-3,4,6-tris-(bis-benzyloxy-phosphanyloxy)-cyclohexyl ester(651313-77-8)

Safety Data

• Hazardous Substances Data: 651313-77-8(Hazardous Substances Data)

Upstream product

• 108549-23-1 Dibenzyl N,N-diisopropylphosphoramidite 
• 141040-66-6 2,5-di-O-phenylmethyl-myo-inositol 

Downstream Products

• 141040-65-5 octabenzyl 1,3,4,6-(2,5-di-O-benzyl-myo-inosityl)tetrakisphosphate 

Relevant articles and documents

Tetrakisphosphates and Bispyrophosphates of myo-Inositol Derivatives as Allosteric Effectors of Human Hemoglobin: Synthesis, Molecular Recognition, and Oxygen Release

Various 2,5- and 1,4-substituted and unsubstituted myo-inositol tetrakisphosphates and bispyrophosphates were prepared following a general synthetic pathway. All final compounds were tested for their capability to induce oxygen release from human hemoglob

The preparation, resolution, and phosphorylation of some benzyl ethers of myo-inositol: Intermediates for the synthesis of myo-inositol phosphates of the phosphatidylinositol cycle

The syntheses of the following chiral compounds are described: 1D-2,3,6-tri-, 1D-2,4,5-tri, 1D-2,5,6-tri-, 1D-1,2,3,4-tetra, 1D-1,2,3,6-tetra-, 1D-1,2,4,5-tetra-, and 1D-2,3,5,6-tetra-0-benzyl-myo-inositol; and 1D-2,5,6-tri-0-benzyl-1-0-p-methoxybenyl- an