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1,3,4,5,6-penta-O-benzyl-2-O-methanesulfonyl myo-inositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108235-14-9

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108235-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108235-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,2,3 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108235-14:
(8*1)+(7*0)+(6*8)+(5*2)+(4*3)+(3*5)+(2*1)+(1*4)=99
99 % 10 = 9
So 108235-14-9 is a valid CAS Registry Number.

108235-14-9Relevant academic research and scientific papers

ACETYLATED PRODRUGS FOR DELIVERY ACROSS THE BLOOD-BRAIN BARRIER

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Page/Page column 35, (2019/11/12)

The present disclosure relates to pharmaceutical compositions including a compound derived from a parent compound having a hydroxyl or amino moiety, wherein the hydroxyl in the parent compound is presented as an ester in the compound or the amino in the parent compound is presented as an amide in the compound, and their use to prevent or treat neurological disease.

Synthesis of phosphatidylinositol analogs containing sulfonylmethylene or methyleneoxy linkages

Elie, C. J. J.,Brounts, D. M.,Dreef, C. E.,Marel, G. A. van der,Boom, J. H. van

, p. 192 - 196 (2007/10/02)

Alkylation of the α-lithio anion of 2,3,4,5,6-penta-O-benzyl-myo-inositol 1-(methane-sulfonate) with 1,2-O-isopropylidene-sn-glycerol 3-(trifluoromethanesulfonate) gave, after removal of the acetonide function followed by palmitoylation and finally hydrog

AN APPROACH TOWARD THE SYNTHESIS OF RACEMIC MYO-INOSITOL 1-( 3,4-DI-PALMITOYLOXYBUTYL)-SULFONATE

Elle, C. J. J.,Dreef, C. E.,Brounts, D. M.,Marel, G. A. van der,Boom, J. H. van

, p. 92 - 94 (2007/10/02)

Substitution of the triflate function in 1,2-isopropylidene-sn-glycerol 3-trifluoromethanesulfonate by the α-lithio-anion of 2,3,4,5,6-penta-O-benzyl-myo-inositol 1-methanesulfonate afforded, after acid hydrolysis of the acetonide function, followed by pa

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