34204-47-2 Usage
Uses
Used in Organic Synthesis:
(1E)-1-(furan-2-yl)-4,4-dimethylpent-1-en-3-one is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its reactivity and structural features facilitate the synthesis of a broad spectrum of compounds, making it a valuable component in the development of new chemical entities.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (1E)-1-(furan-2-yl)-4,4-dimethylpent-1-en-3-one is utilized as a starting material for the design and synthesis of potential drug candidates. Its biological activities, such as anti-inflammatory, antifungal, and antibacterial properties, make it a promising candidate for the development of new therapeutic agents.
Used in Pharmaceutical Development:
(1E)-1-(furan-2-yl)-4,4-dimethylpent-1-en-3-one is used as a building block in the pharmaceutical industry for the development of new drugs. Its potential biological activities and chemical properties make it a valuable component in the creation of innovative medications to address various health conditions.
Used in Agrochemicals:
(1E)-1-(furan-2-yl)-4,4-dimethylpent-1-en-3-one is also used in the agrochemical industry as a precursor for the development of new pesticides and other agricultural chemicals. Its antifungal and antibacterial properties are particularly useful in this context, contributing to the creation of effective solutions for crop protection and management.
Overall, (1E)-1-(furan-2-yl)-4,4-dimethylpent-1-en-3-one is a multifaceted chemical compound with a diverse range of applications across different industries, including organic synthesis, medicinal chemistry, pharmaceuticals, and agrochemicals. Its unique properties and potential make it a valuable asset in the ongoing pursuit of scientific advancements and innovations.
Check Digit Verification of cas no
The CAS Registry Mumber 34204-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,0 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34204-47:
(7*3)+(6*4)+(5*2)+(4*0)+(3*4)+(2*4)+(1*7)=82
82 % 10 = 2
So 34204-47-2 is a valid CAS Registry Number.
34204-47-2Relevant academic research and scientific papers
Synthesis of Vicinal Quaternary All-Carbon Centers via Acid-catalyzed Cycloisomerization of Neopentylic Epoxides
Schmid, Matthias,Sokol, Kevin R.,Wein, Lukas A.,Torres Venegas, Sofia,Meisenbichler, Christina,Wurst, Klaus,Podewitz, Maren,Magauer, Thomas
supporting information, p. 6526 - 6531 (2020/09/02)
We report our studies on the development of a catalytic cycloisomerization of 2,2-disubstituted neopentylic epoxides to produce highly substituted tetralins and chromanes. Termination of the sequence occurs via Friedel-Crafts-type alkylation of the remote (hetero)arene linker. The transformation is efficiently promoted by sulfuric acid and proceeds best in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as the solvent. Variation of the substitution pattern provided detailed insights into the migration tendencies and revealed a competing disproportionation pathway of dihydronaphthalenes.
Enantioselective Copper-Catalyzed 1,5-Cyanotrifluoromethylation of Vinylcyclopropanes
Zhang, Zi-Qi,Meng, Xiang-Yu,Sheng, Jie,Lan, Quan,Wang, Xi-Sheng
supporting information, p. 8256 - 8260 (2019/10/16)
A copper-catalyzed enantioselective 1,5-cyanotrifluoromethylation of vinylcyclopropanes has been developed using a radical relay strategy. This asymmetric reaction has demonstrated high enantioselective control, broad substrate scope, and mild conditions. Initiated by the in situ generated CF3 radical from Togni's reagent, this method offers a new solution for remote enantioselective bifunctionalization of alkenes and thus provides a straightforward way for the synthesis of chiral CF3-containing internal alkenylnitriles.
