13057-19-7 Usage
Description
Iodomethyl methyl ether, also known as Iodomethoxymethane, is a halo ether commonly used in various chemical reactions and processes. It is characterized by its ability to undergo methoxymethylation reactions with phosphorus, carbon, oxygen, and nitrogen-containing nucleophiles. This versatile compound is synthesized by reacting methylal (dimethoxymethane) with iodotrimethylsilane and contains copper as a stabilizer. Its molecular structure has been studied through microwave spectral analysis, providing insights into its rotational, centrifugal distortion constants, and the nuclear electric quadrupole coupling constant tensor.
Uses
Used in Chemical Synthesis:
Iodomethyl methyl ether is used as a reagent in the chemical synthesis of various compounds. Its ability to undergo methoxymethylation reactions with different nucleophiles makes it a valuable tool in the creation of new molecules and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, iodomethyl methyl ether is used as an intermediate in the synthesis of various drugs and drug candidates. Its versatility in chemical reactions allows for the development of new therapeutic agents with potential applications in treating various diseases and conditions.
Used in Research and Development:
Iodomethyl methyl ether is also utilized in research and development settings, where it serves as a key component in the study of chemical reactions and the development of new synthetic methods. Its unique properties and reactivity make it an essential tool for chemists and researchers working on the design and synthesis of novel compounds.
Used in Analytical Chemistry:
In analytical chemistry, iodomethyl methyl ether can be employed as a derivatizing agent for the analysis of various compounds. Its ability to react with different functional groups allows for the modification and detection of target molecules, enhancing the sensitivity and accuracy of analytical techniques.
Used in Material Science:
Iodomethyl methyl ether can be used in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its role in methoxymethylation reactions can lead to the creation of novel materials with potential applications in various industries, including electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 13057-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13057-19:
(7*1)+(6*3)+(5*0)+(4*5)+(3*7)+(2*1)+(1*9)=77
77 % 10 = 7
So 13057-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C2H5IO/c1-4-2-3/h2H2,1H3
13057-19-7Relevant articles and documents
Dual Reactivity of Methoxymethyl Benzenesulfonate in Nucleophilic Substitution
Okuyama, Tadashi,Fueno, Takayuki
, p. 2672 - 2683 (2007/10/02)
Hydrolysis of methoxymethyl benzenesulfenate is catalyzed by both acid and base.Acid-catalyzed hydrolysis is further accelerated by various nucleophiles like halide ions, thiocyanate, dialkyl sulfide, and the substrate itself.The catalytic constants coincide with those for ethyl benzenesulfenate within 2-fold in magnitude.The nucleophilic reactivity strongly suggests the reaction at the sulfenyl sulfur, but examination of the products from the 18O-labeled substrate showed that the bond cleavage occurs mostly between the oxygen and the proformyl carbon except for the acid-catalyzed water reaction which undergoes the S-O cleavage.A mechanism for a nucleophilic reaction at the sulfur to form a sulfurane intermediate which breaks down with the C-O cleavage is presented.The hydrolysis rate is also strongly dependent on the second order of buffer concentrations in carboxylate and tertiary amine buffer solutions.The third-order term involves both the general acid and the conjugate base of the buffer, and the latter reacts at the sulfur as a nucleophile in the rate-determining step but leads to the C-O cleavage in the same way as the other catalytic nucleophiles.
