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4-O-benzyloxymethyl-myo-inosytol 1,3,5-orthoformate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135556-68-2

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135556-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135556-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,5 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135556-68:
(8*1)+(7*3)+(6*5)+(5*5)+(4*5)+(3*6)+(2*6)+(1*8)=142
142 % 10 = 2
So 135556-68-2 is a valid CAS Registry Number.

135556-68-2Relevant academic research and scientific papers

Synthesis of 2-substituted myo-inositol 1,3,4,5-tetrakis(phosphate) and 1,3,4,5,6-pentakis(phosphate) analogs

Ozaki,Koga,Ling,Watanabe,Kimura,Hirata

, p. 1058 - 1063 (1994)

Some biologically interesting inositol poly(phosphate) derivatives, 2-O-(P-aminobenzoyl)-myo-inositol 1,3,4,5-tetrakis(phosphate), 2-O-(4-aminocyclohexylcarbonyl)-myo-inositol 1,3,4,5-tetrakis(phosphate), myo-inositol 1,3,4,5,6-pentakis(phosphate), and its 2-substituted analogs, were synthesized. Inositol tetrakis(phosphate) and pentakis(phosphate) affinity columns were also prepared. The inositol 1,3,4,5-tetrakis(phosphate) affinity column was found to be effective in isolating the binding proteins from bovine cardiac membranes.

The Total Synthesis of myo-Inositol Phosphates via myo-Inositol Orthoformate

Billington, David C.,Baker, Raymond,Kulagowski, Janusz J.,Mawer, Ian M.,Vacca, Joseph P.,et al.

, p. 1423 - 1429 (2007/10/02)

Novel selective alkylations of myo-inositol orthoformate (4) have been used to prepare a series of protected myo-inositol derivatives, (5a-e), (7), (10), (12), and (16).These intermediates have been used in efficient total syntheses of myo-inositol 2-phosphate, (9); myo-inositol 4-phosphate, (6); myo-inositol 1,3-bisphosphate, (18); and myo-inositol 1,3,4,5-tetrakisphosphate (14).This report represents the first total synthesis of the important natural metabolites (14) and (18) and significantly improved methods of preparation of (6) and (9).

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