153265-90-8 Usage
Type
Synthetic chemical compound
Derivation
Derived from myo-inositol
Structure
A derivative of inositol with a butyryl group at position 1 and two benzoyl groups at positions 4 and 6
Usage
Commonly used as a reagent in organic chemistry reactions, particularly in the synthesis of inositol derivatives and other organic compounds
Application
Used as a building block for the creation of various pharmaceuticals and biologically active molecules
Industries
Potential applications in the food and cosmetic industries, as well as in medical research for its properties and functions in the human body.
Check Digit Verification of cas no
The CAS Registry Mumber 153265-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153265-90:
(8*1)+(7*5)+(6*3)+(5*2)+(4*6)+(3*5)+(2*9)+(1*0)=128
128 % 10 = 8
So 153265-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C32H25NO4/c34-31(35)30(18-28-22-11-3-1-9-20(22)17-21-10-2-4-12-23(21)28)33-32(36)37-19-29-26-15-7-5-13-24(26)25-14-6-8-16-27(25)29/h1-17,29-30H,18-19H2,(H,33,36)(H,34,35)/t30-/m0/s1
153265-90-8Relevant articles and documents
Enzyme assisted synthesis of D-myo-inositol-1,2,6-trisphosphate
Andersch,Schneider
, p. 349 - 352 (2007/10/03)
The title compound is prepared in enantiomerically pure form via a facile enzyme assisted route. Essential for the success of the described method were a) the highly enantioselective esterification of 4,6-O-dibenzoyl-myo-inositol 2, b) the selective acylation of the axial hydroxyl function in 3 and c) the selective, base catalysed methanolysis of one benzoate group in 5. The obtained, selectively protected 1,2,6-triol 6 was converted into the title compound 7 by phosphorylation using N,N-dimethyl dibenzyl phosphoamidite followed by deprotection.
