932-62-7 Usage
Description
3-Acetyl-1-methylpyrrole is an organic compound with the molecular formula C6H7NO. It is a derivative of the pyrrole ring system, featuring a methyl group and an acetyl group attached to the pyrrole nucleus. 3-ACETYL-1-METHYLPYRROLE has been studied for its enthalpy of formation in both condensed and gas phases, indicating its potential applications in various chemical and industrial processes.
Uses
Used in Chemical Synthesis:
3-Acetyl-1-methylpyrrole is used as a synthetic intermediate for the production of various organic compounds and pharmaceuticals. Its unique structure allows it to be a versatile building block in the synthesis of complex organic molecules, including potential drug candidates and specialty chemicals.
Used in Material Science:
In the field of material science, 3-acetyl-1-methylpyrrole can be utilized as a component in the development of novel materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with tailored characteristics, such as improved thermal stability or enhanced electrical conductivity.
Used in Analytical Chemistry:
3-Acetyl-1-methylpyrrole can be employed as a reference compound or a standard in analytical chemistry for the calibration of instruments and the development of new analytical methods. Its distinct chemical properties make it suitable for use in various analytical techniques, such as chromatography, spectroscopy, and mass spectrometry.
Used in Research and Development:
As a compound with unique structural features, 3-acetyl-1-methylpyrrole is used in research and development for exploring its potential applications and properties. Scientists and researchers can investigate its reactivity, stability, and interactions with other molecules, which can lead to the discovery of new applications and insights into its behavior.
Synthesis Reference(s)
The Journal of Organic Chemistry, 46, p. 839, 1981 DOI: 10.1021/jo00318a002
Check Digit Verification of cas no
The CAS Registry Mumber 932-62-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 932-62:
(5*9)+(4*3)+(3*2)+(2*6)+(1*2)=77
77 % 10 = 7
So 932-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO/c1-6(9)7-3-4-8(2)5-7/h3-5H,1-2H3
932-62-7Relevant articles and documents
Photo-on-Demand Synthesis of Vilsmeier Reagents with Chloroform and Their Applications to One-Pot Organic Syntheses
Liang, Fengying,Eda, Kazuo,Okazoe, Takashi,Wada, Akihiro,Mori, Nobuaki,Konishi, Katsuhiko,Tsuda, Akihiko
, p. 6504 - 6517 (2021/05/06)
The Vilsmeier reagent (VR), first reported a century ago, is a versatile reagent in a variety of organic reactions. It is used extensively in formylation reactions. However, the synthesis of VR generally requires highly toxic and corrosive reagents such as POCl3, SOCl2, or COCl2. In this study, we found that VR is readily obtained from a CHCl3 solution containing N,N-dimethylformamide or N,N-dimethylacetamide upon photo-irradiation under O2 bubbling. The corresponding Vilsmeier reagents were obtained in high yields with the generation of gaseous HCl and CO2 as byproducts to allow their isolations as crystalline solid products amenable to analysis by X-ray crystallography. With the advantage of using CHCl3, which bifunctionally serves as a reactant and a solvent, this photo-on-demand VR synthesis is available for one-pot syntheses of aldehydes, acid chlorides, formates, ketones, esters, and amides.
