68473-30-3 Usage
Uses
Used in Polymer and Copolymer Production:
METHYL VINYL ETHER (METHYL-D3) is used as a monomer for the production of polymers and copolymers, contributing to the development of materials with specific properties tailored for various applications.
Used in Chemical Reactions:
As a reactive solvent, METHYL VINYL ETHER (METHYL-D3) is used in various chemical reactions to facilitate or enhance the processes, leading to the formation of desired products.
Used in Organic Compound Synthesis:
METHYL VINYL ETHER (METHYL-D3) is used as a precursor in the synthesis of other organic compounds, enabling the creation of a wide range of chemical products.
Used in Pharmaceutical and Agrochemical Production:
METHYL VINYL ETHER (METHYL-D3) is used as a reagent in the production of pharmaceuticals and agrochemicals, playing a crucial role in the development of new drugs and agricultural products.
Used in Nuclear Magnetic Resonance (NMR) Spectroscopy:
As a deuterated form of methyl vinyl ether, METHYL VINYL ETHER (METHYL-D3) is used in NMR spectroscopy studies, providing valuable insights into the structure and dynamics of molecules, which is essential for understanding their properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 68473-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68473-30:
(7*6)+(6*8)+(5*4)+(4*7)+(3*3)+(2*3)+(1*0)=153
153 % 10 = 3
So 68473-30-3 is a valid CAS Registry Number.
68473-30-3Relevant academic research and scientific papers
REARRANGEMENT AND METHYL LOSS FROM IONIZED PROPENE OXIDE AND METHYL VINYL ETHER.
Turecek,McLafferty
, p. 2528 - 2531 (2007/10/02)
Molecular cations of propene oxide (a) and methyl vinyl ether (b), despite a large difference (35 kcal mol** minus **1) in their heats of formation, undergo two very similar metastable methyl loss dissociations; for both of these dissociations a and b exhibit the same kinetic energy release values and produce acetyl ions. Deuterium labeling shows that a ions undergo little direct methyl loss, but instead isomerize by ring opening and 1,4-H transfer to b. For long-lived ions of energies below the decomposition threshold, nearly complete hydrogen exchange occurs between the methyl and methylene groups.
