61621-47-4 Usage
Description
2,5-DIMETHYLCYCLOHEXANE-1,3-DIONE, also known as dimedone, is a cyclic ketone compound with the molecular formula C8H12O2. It is a white crystalline solid with a camphor-like odor and is commonly used as a reagent in organic synthesis. Dimedone is known for its ability to form useful adducts with various compounds, particularly with carbonyl compounds, making it useful in the formation of cyclic compounds.
Uses
Used in Organic Synthesis:
2,5-DIMETHYLCYCLOHEXANE-1,3-DIONE is used as a reagent for the synthesis of various organic compounds due to its ability to form adducts with carbonyl compounds, which aids in the formation of cyclic compounds.
Used in Pharmaceutical Synthesis:
2,5-DIMETHYLCYCLOHEXANE-1,3-DIONE is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Agrochemical Synthesis:
2,5-DIMETHYLCYCLOHEXANE-1,3-DIONE is used as a reagent in the synthesis of agrochemicals, helping to create compounds for agricultural applications such as pesticides and herbicides.
Used in Antioxidant Applications:
2,5-DIMETHYLCYCLOHEXANE-1,3-DIONE has been studied for its potential antioxidant properties, which could be utilized in various industries to prevent oxidation and spoilage.
Used in Antimicrobial Applications:
2,5-DIMETHYLCYCLOHEXANE-1,3-DIONE has been studied for its potential antimicrobial properties, which could be applied in industries where controlling microbial growth is essential, such as in food preservation or medical settings.
Check Digit Verification of cas no
The CAS Registry Mumber 61621-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,2 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61621-47:
(7*6)+(6*1)+(5*6)+(4*2)+(3*1)+(2*4)+(1*7)=104
104 % 10 = 4
So 61621-47-4 is a valid CAS Registry Number.
61621-47-4Relevant articles and documents
TETRAHYDRONAPHTHALENE DERIVATIVES USEFUL AS NRF2 ACTIVATORS
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Page/Page column 113, (2019/06/11)
Provided are compounds of Formula I, or pharmaceutically acceptable salts thereof, and methods for their use as Nrf2 activators and for their production.
Catalytic decarboxylative alkenylation of enolates
Schroeder, Sybrin P.,Taylor, Nicholas J.,Jackson, Paula,Franckevicius, Vilius
supporting information, p. 3778 - 3781 (2013/08/23)
A palladium-catalyzed decarboxylative alkenylation of stabilized enolates has been developed, which gives rise to alkenylated dicarbonyl products from enol carbonates regioselectively with concomitant installation of a quaternary all-carbon center. The broad scope of the reaction has been demonstrated by successfully utilizing a range of enolates and external phenol nucleophiles.
Intramolecular Additions of Allylsilanes to Conjugated Dienones. The Synthesis of Three Perforanes
Majetich, George,Defauw, Jean,Ringold, Clay
, p. 50 - 68 (2007/10/02)
Intramolecular addition of allylsilanes to 3-vinylcycloalkenones provides a powerful means of constructing functionalized 5-5, 5-7, 6-5, and 6-7 bicyclic ring systems.Our results reveal a divergence in reactivity, dependent on reaction catalyst and substr