2032-45-3 Usage
Description
(6Z)-6-[morpholin-4-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one is a complex organic molecule characterized by its cyclohexadienone backbone and a morpholine-4-yl(sulfanyl)methylidene group attached to it. The "(6Z)" in its name signifies the presence of a specific geometric isomerism, which may contribute to its unique properties and potential reactivity. (6Z)-6-[morpholin-4-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one holds promise for applications in organic synthesis and medicinal chemistry, although further research is required to fully comprehend its characteristics and possible uses.
Uses
Used in Organic Synthesis:
(6Z)-6-[morpholin-4-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one is used as an intermediate in the synthesis of various organic compounds due to its unique structure and potential reactivity. Its ability to participate in different chemical reactions makes it a valuable building block for creating novel molecules with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6Z)-6-[morpholin-4-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one is used as a starting material for the development of new pharmaceuticals. Its distinct structural features may allow for the design of innovative drugs with improved efficacy and selectivity, targeting a wide range of therapeutic areas.
Used in Pharmaceutical Research:
(6Z)-6-[morpholin-4-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one is utilized in pharmaceutical research as a potential candidate for drug discovery. Its unique chemical properties and reactivity may lead to the development of new therapeutic agents with novel mechanisms of action, addressing unmet medical needs and contributing to the advancement of healthcare.
Used in Chemical Industry:
Within the chemical industry, (6Z)-6-[morpholin-4-yl(sulfanyl)methylidene]cyclohexa-2,4-dien-1-one may find applications in the production of specialty chemicals, materials, and additives. Its specific geometric isomerism and reactivity could be harnessed to create high-value products with tailored properties for various applications, such as coatings, adhesives, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 2032-45-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2032-45:
(6*2)+(5*0)+(4*3)+(3*2)+(2*4)+(1*5)=43
43 % 10 = 3
So 2032-45-3 is a valid CAS Registry Number.
2032-45-3Relevant articles and documents
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.].
Microwave-assisted rapid hydrolysis and preparation of thioamides by Willgerodt-Kindler reaction
Matloubi Moghaddam,Ghaffarzadeh
, p. 317 - 321 (2007/10/03)
Aldehydes and aryl alkyl ketones were efficiently transformed to thioamides with the same number of carbon atoms via Willgerodt-Kindler reaction under microwave irradiation in solvent-free conditions. The thioamides obtained were hydrolyzed to corresponding carboxylic acids with microwave dielectric heating in one minute. Both reactions are very fast and the yields are excellent.
