61266-71-5 Usage
Description
2-methyl-2-hydroxymethyloxetane, also known as 2M2HMO, is a versatile chemical compound characterized by its clear, colorless liquid form with a mild odor and low volatility. It is commonly utilized as a solvent or co-solvent across various industries due to its unique chemical properties, making it a valuable ingredient in numerous industrial and commercial processes.
Uses
Used in Coatings and Adhesives Industry:
2-methyl-2-hydroxymethyloxetane is used as a solvent or co-solvent for its suitability in high solids coatings and adhesives, attributed to its low volatility which helps in creating stable and high-quality formulations.
Used in Cleaning Formulations:
In the cleaning industry, 2-methyl-2-hydroxymethyloxetane is used as a component in cleaning formulations, leveraging its ability to dissolve a wide range of substances and contribute to the effectiveness of the cleaning products.
Used in Pharmaceutical Production:
2-methyl-2-hydroxymethyloxetane is utilized as a component in the production of pharmaceuticals, where its chemical properties are harnessed to aid in the manufacturing process of various medicinal compounds.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 2-methyl-2-hydroxymethyloxetane is used in the production of agrochemicals, playing a role in the synthesis of substances that contribute to agricultural productivity and pest control.
Check Digit Verification of cas no
The CAS Registry Mumber 61266-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,6 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61266-71:
(7*6)+(6*1)+(5*2)+(4*6)+(3*6)+(2*7)+(1*1)=115
115 % 10 = 5
So 61266-71-5 is a valid CAS Registry Number.
61266-71-5Relevant articles and documents
TRANSPOSITION DES OXIRANNES-ETHANOLS PAR L'INTERMEDIAIRE D'ALCOXYETAINS
Bats, J. -P.,Moulines, J.,Picard, P.,Leclercq, D.
, p. 2139 - 2146 (2007/10/02)
Oxiraneethoxytributyltins prepared from the corresponding oxiraneethanols, on heating at 200 deg C gave, after demetalation with isophthalic acid, 2-oxetanemethanols and/or 3-oxolanols.As appears from about thirty rearrangements the choice between oxetane and oxolane formation is dependent on: (1) the relative degree of substitution of the oxirane ring; cyclization occuring predominantly at the more substituted carbon; and (2) the configuration of the oxirane ring, when both its ends are equally substituted; cis form being more suitable for genaration of the smaller ring.The reaction is shown to proceed with inversion of configuration at the site of oxygen attack.The results of attempts to perform the rearrangement in dilute-phase or throught alkaline metal alkoxides in various media support the conclusion that there is a large contribution by electrophilic assistance to the oxirane ring opening.Such assistance can be efficiently provided by a tin atom in a push-pull mechanism which accomodates all the facts.The present method of oxiraneethanol rearrangement may offer a convenient route to functional oxetanes.