163041-47-2 Usage
Description
(Z)-Methyl 2-iodo-3-methoxyacrylate, with the chemical formula C6H9IO3, is a clear, colorless liquid chemical compound. It is predominantly utilized as an intermediate in the synthesis of organic compounds, making it a valuable component in the creation of various bioactive molecules.
Uses
Used in Pharmaceutical Industry:
(Z)-Methyl 2-iodo-3-methoxyacrylate is used as a building block for the production of bioactive molecules, contributing to the development of new pharmaceuticals. Its unique chemical properties and reactivity make it a promising candidate for creating innovative drugs and therapies.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (Z)-Methyl 2-iodo-3-methoxyacrylate serves as a key intermediate in the synthesis of bioactive compounds, which can be used in the development of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Academic Research:
(Z)-Methyl 2-iodo-3-methoxyacrylate is also employed in academic research settings due to its distinctive chemical characteristics and reactivity. Researchers use this compound to explore new reactions, mechanisms, and potential applications in various fields of chemistry and materials science.
Safety Precautions:
It is crucial to handle (Z)-Methyl 2-iodo-3-methoxyacrylate with care, as it is potentially hazardous. To minimize risks, it should be managed and stored according to the best laboratory practices, ensuring the safety of both the researchers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 163041-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,0,4 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 163041-47:
(8*1)+(7*6)+(6*3)+(5*0)+(4*4)+(3*1)+(2*4)+(1*7)=102
102 % 10 = 2
So 163041-47-2 is a valid CAS Registry Number.
163041-47-2Relevant articles and documents
MICROBIOCIDAL COMPOUNDS
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Page/Page column 53-54, (2021/11/13)
Compounds of the formula (I), wherein the substituents are as defined in claim 1, useful as a pesticides, especially as fungicides.
MICROBIOCIDAL COMPOUNDS
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Page/Page column 60-61, (2021/11/06)
Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially as fungicides.
Dehydration-type Ti-Claisen Condensation (Carbonhomologation) of α-Heteroatom-substituted Acetates with Alkyl Formates: Utilization as (Z)-Stereodefined Cross-coupling Partners and Application to Concise Synthesis of Strobilurin A
Nakatsuji, Hidefumi,Kamada, Risa,Kitaguchi, Hideya,Tanabe, Yoo
, p. 3865 - 3879 (2017/11/15)
TiCl4?Et3N or ?Bu3N reagent conducted a highly (Z)-stereoselective carbon homologation (dehydration type Ti-Claisen condensation) of alkyl α-heteroatom (halo and sulfonyloxy)-substituted acetates (XCH2CO2R) with alkyl formates (HCO2R) to afford various alkyl β-alkoxy-α-halo or sulfonyloxy-substituted acrylates (24 examples; 51%–91% yield). Stereoretentive Suzuki-Miyaura, Negishi, and Sonogashira cross-couplings using the obtained methyl β-methoxy-α-halo or sulfonyloxy-substituted acrylates proceeded smoothly to produce a variety of β-alkoxy-α-substituted acrylates in moderate to high yield (35 examples; 29%–99% yield). As a successful application, a 3-step straightforward synthesis of strobilurin A was performed utilizing the present reaction sequence (dehydration type Ti-Claisen condensation and Suzuki-Miyaura cross-coupling), wherein the geometry of the three consecutive olefins (2E,3Z,5E) was completely maintained. (Figure presented.).
