57954-41-3 Usage
Uses
Used in Organic Synthesis:
(2-methoxyphenyl)(morpholin-4-yl)methanethione is used as a building block for the synthesis of complex organic molecules. Its unique structure allows for versatile chemical reactions, enabling the creation of a wide range of compounds with potential applications in various industries.
Used in Pharmaceutical Development:
(2-methoxyphenyl)(morpholin-4-yl)methanethione is used as a key intermediate in the development of new pharmaceuticals. Its presence in a molecule can impart specific biological activities, making it a valuable component in the design and synthesis of novel drugs with potential therapeutic benefits.
Used in Chemical Research:
(2-methoxyphenyl)(morpholin-4-yl)methanethione is used as a research tool in the study of chemical reactions and mechanisms. Its unique properties allow scientists to gain insights into the behavior of thioether compounds and their interactions with other molecules, contributing to the advancement of chemical knowledge.
Used in Material Science:
(2-methoxyphenyl)(morpholin-4-yl)methanethione is used in the development of new materials with specific properties. Its incorporation into polymers or other materials can result in materials with improved characteristics, such as enhanced stability, reactivity, or selectivity, making them suitable for various applications.
Used in Agrochemicals:
(2-methoxyphenyl)(morpholin-4-yl)methanethione is used as an active ingredient or intermediate in the development of agrochemicals, such as pesticides or herbicides. Its unique structure and properties can contribute to the effectiveness of these products, helping to improve crop yields and protect against pests.
Used in Flavor and Fragrance Industry:
(2-methoxyphenyl)(morpholin-4-yl)methanethione is used as a component in the creation of unique flavors and fragrances. Its distinct chemical structure can impart specific olfactory properties, making it a valuable addition to the palette of scents and tastes available to the industry.
Check Digit Verification of cas no
The CAS Registry Mumber 57954-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57954-41:
(7*5)+(6*7)+(5*9)+(4*5)+(3*4)+(2*4)+(1*1)=163
163 % 10 = 3
So 57954-41-3 is a valid CAS Registry Number.
57954-41-3Relevant academic research and scientific papers
Sulfated polyborate catalyzed Kindler reaction: a rapid, efficient, and green protocol
Khatri, Chetan K.,Mali, Anil S.,Chaturbhuj, Ganesh U.
, p. 1463 - 1468 (2017/07/18)
A rapid, green, and efficient one-pot, three-component Kindler reaction was developed using a sulfated polyborate catalyst. The method described the reaction of aldehydes, amines/ammonium acetate, and sulfur for the synthesis of thioamides using sulfated polyborate under a solvent free condition at 100?°C. The key features of the present protocol are high yields, short reaction time, easy workup, and recyclability of a catalyst which gives economical as well as ecological rewards. The present method also has an ability to tolerate a variety of functional groups. Graphical abstract: [Figure not available: see fulltext.].
Extension of the Willgerodt-Kindler reaction: Protected carbonyl compounds as efficient substrates for this reaction
Darabi, Hossein Reza,Aghapoor, Kioumars,Tajbakhsh, Mahmoud
, p. 4167 - 4169 (2007/10/03)
Nitrogen derivatives of carbonyl compounds such as oximes, hydrazones, and semicarbazones were found to be excellent candidates for the Willgerodt-Kindler reaction. They can be used directly in a solvent-free reaction, under both classical and microwave conditions, to give the corresponding thiomorpholides in good yields.
