131233-70-0 Usage
Chemical compound
A chemical compound that belongs to the group of inositols, which are a group of carbocyclic polyols.
Derivative of myoinositol
A derivative of myoinositol, which is a key component of cell membranes and is involved in various biological processes such as cell signaling and nerve transmission.
Benzyl groups addition
The addition of benzyl groups to the inositol molecule increases its lipophilicity, or its ability to dissolve in fats and oils.
Usefulness
This increased lipophilicity can make 1,5,6-tri-O-benzylmyoinositol more useful for certain applications such as drug delivery.
Application in organic synthesis
1,5,6-tri-O-benzylmyoinositol is used in organic synthesis and medicinal chemistry.
Building block
It serves as a building block for the production of various pharmaceuticals and bioactive compounds.
Unique structure and properties
Its unique structure and properties make it a valuable tool in the field of chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 131233-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,3 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 131233-70:
(8*1)+(7*3)+(6*1)+(5*2)+(4*3)+(3*3)+(2*7)+(1*0)=80
80 % 10 = 0
So 131233-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C27H30O6/c28-22-23(29)25(31-16-19-10-4-1-5-11-19)27(33-18-21-14-8-3-9-15-21)26(24(22)30)32-17-20-12-6-2-7-13-20/h1-15,22-30H,16-18H2/t22?,23-,24-,25-,26+,27?/m1/s1
131233-70-0Relevant articles and documents
Novel synthesis of enantiomerically pure natural inositols and their diastereoisomers
Takahashi,Kittaka,Ikegami
, p. 2705 - 2716 (2007/10/03)
The various inositol polyphosphates have been found to trigger many important biological processes. Although the knowledge of this phosphoinositide signaling system has been discovered in the past 10 years, many factors remain unclear. For this reason, there is an increased demand for supplies of D-myo-inositol and particularly of novel analogues to investigate these biological mechanisms in more detail. Herein, we report the efficient syntheses of all diastereoisomers of inositol starting with 6-O-acetyl-5-enopyranosides. Conversion of 6-O-acetyl-5-enopyranosides into the corresponding substituted cyclohexanones (Ferrier-II rearrangement) was found to proceed efficiently with a catalytic amount of palladium dichloride. Stereoselective reduction of β-hydroxy ketones obtained provided the precursors to all inositol diastereoisomers in good to excellent yields and with high stereoselectivities. Good accessibility of these enantiomerically pure inositol diastereoisomers results in the efficient syntheses of D-myo-inositol 1,4,5-trisphosphate and D-myo-inositol 1,3,4,5-tetrakisphosphate.