45734-41-6 Usage
Description
(3-tert-butyl-2-methyloxiran-2-yl)methanol (non-preferred name), also known as tert-Butyl glycidyl ether, is a chemical compound with the formula C8H16O2. It is a colorless liquid with a faint, sweet odor and is commonly used as a stabilizer and plasticizer in the production of polyvinyl chloride (PVC) and other polymers. It can also be used as a reactive diluent in epoxy resins and as a solvent for organic synthesis. However, it is important to use the correct systematic name, tert-Butyl glycidyl ether, in order to accurately identify and describe the chemical. Its precise chemical structure and properties make it useful in various industrial applications, but it is important to handle it with care due to its potential health and environmental hazards.
Uses
Used in Plastics and Polymer Industry:
(3-tert-butyl-2-methyloxiran-2-yl)methanol (non-preferred name) is used as a stabilizer and plasticizer for polyvinyl chloride (PVC) and other polymers to improve their flexibility, durability, and resistance to degradation.
Used in Epoxy Resin Industry:
(3-tert-butyl-2-methyloxiran-2-yl)methanol (non-preferred name) is used as a reactive diluent in epoxy resins to reduce viscosity, improve processability, and enhance the mechanical and chemical properties of the final product.
Used in Organic Synthesis:
(3-tert-butyl-2-methyloxiran-2-yl)methanol (non-preferred name) is used as a solvent for various organic synthesis processes, enabling the production of a wide range of chemical compounds and intermediates.
Check Digit Verification of cas no
The CAS Registry Mumber 45734-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,7,3 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 45734-41:
(7*4)+(6*5)+(5*7)+(4*3)+(3*4)+(2*4)+(1*1)=126
126 % 10 = 6
So 45734-41-6 is a valid CAS Registry Number.
45734-41-6Relevant articles and documents
Photooxygenation of olefins in the presence of titanium(IV) catalyst: A convenient 'one-pot' synthesis of epoxy alcohols
Adam,Braun,Griesbeck,Lucchini,Staab,Will
, p. 203 - 212 (2007/10/02)
The photooxygenation of olefins in the presence of transition-metal complexes derived from Ti, V, and Mo constitutes a convenient and efficient 'one-pot' synthesis of epoxy alcohols. First, singlet oxygen transforms the olefin via an ene reaction into its allylic hydroperoxide, and subsequently, the allylic hydroperoxide is converted via transition-metal-catalyzed oxygen transfer into its epoxy alcohol. From the point of view of the olefinic substrate, the oxygen transfer is intermolecular, one allylic hydroperoxide molecule serving as oxygen donor and the other as oxygen acceptor in the form of its allylic alcohol, the transition metal playing the role of a template for both as in the Sharpless epoxidation. Unlike the latter process, the hydroperoxide donor and the allylic alcohol acceptor are generated in situ and continually consumed via a novel oxygen-transfer chain sequence.
