338458-96-1 Usage
Uses
Used in Pharmaceutical Industry:
2-(IodoMethyl)-6-[(phenylMethoxy)Methyl]-1,4-dioxane is used as a precursor in the preparation of cyclic oligoglycerols, which serve as standards for quality control and analysis in the pharmaceutical industry. These cyclic oligoglycerols are essential for the development and testing of new drugs and therapies, ensuring their safety and efficacy.
Used in Research and Development:
In the field of research and development, 2-(IodoMethyl)-6-[(phenylMethoxy)Methyl]-1,4-dioxane is utilized as a key intermediate in the synthesis of various complex organic compounds. Its unique structure allows for the creation of new molecules with potential applications in various industries, including pharmaceuticals, materials science, and chemical engineering.
Used in Quality Control:
2-(IodoMethyl)-6-[(phenylMethoxy)Methyl]-1,4-dioxane is also used in the quality control processes of cyclic oligoglycerols. It helps in the development of accurate and reliable analytical methods for the assessment of these compounds, ensuring their purity and consistency in pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 338458-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,4,5 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 338458-96:
(8*3)+(7*3)+(6*8)+(5*4)+(4*5)+(3*8)+(2*9)+(1*6)=181
181 % 10 = 1
So 338458-96-1 is a valid CAS Registry Number.
338458-96-1Relevant academic research and scientific papers
Original synthesis of linear, branched and cyclic oligoglycerol standards
Cassel, Stephanie,Debaig, Catherine,Benvegnu, Thierry,Chaimbault, Patrick,Lafosse, Michel,Plusquellec, Daniel,Rollin, Patrick
, p. 875 - 896 (2007/10/03)
A variety of authentic standards of linear, branched and cyclic oligomers of glycerol, with well-defined structures and degrees of polymerisation from 2 to 5, have been efficiently synthesised. Linear oligomers were obtained by means of a convergent approach based on regioselective opening of bis(epoxides) with solketal; branched compounds were synthesised using oxidative cleavage of the corresponding anhydrohexitols as the key step. A 6-exo-trig halocyclisation reaction involving heteroatom-tethered unsaturated alcohols permitted an efficient synthesis of the precursors of selected cyclic dimers; larger cyclic oligomers were prepared by two one-pot Williamson reactions using a ditriflate derived from diglycerol. All these methodologies permitted further scaling up.
