109482-98-6 Usage
General Description
The chemical (1E,4E)-1-(Dimethylamino)-5-(2-furyl)penta-1,4-dien-3-one is a compound with the molecular formula C12H15NO2. It is a penta-1,4-dien-3-one derivative with a dimethylamino group and a furyl group attached to the pentadienone backbone. (1E,4E)-1-(Dimethylamino)-5-(2-furyl)penta-1,4-dien-3-one has potential pharmaceutical applications due to its structural features, such as the presence of a furan ring and a dimethylamino group, which are known to exhibit biological activity. It may be used as a building block in the synthesis of organic compounds or as a precursor for the preparation of pharmaceuticals or agrochemicals. Further research and evaluation of its properties and potential applications are necessary to fully understand the significance of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 109482-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109482-98:
(8*1)+(7*0)+(6*9)+(5*4)+(4*8)+(3*2)+(2*9)+(1*8)=146
146 % 10 = 6
So 109482-98-6 is a valid CAS Registry Number.
109482-98-6Relevant articles and documents
Regioselective Formal [4 + 2] Cycloadditions of Enaminones with Diazocarbonyls through RhIII-Catalyzed C-H Bond Functionalization
Zhou, Shuguang,Yan, Bi-Wei,Fan, Shuai-Xin,Tian, Jie-Sheng,Loh, Teck-Peng
, p. 3975 - 3979 (2018)
A regioselective formal [4 + 2] cycloaddition for the assembly of highly functionalized benzene rings was successfully developed. In this reaction, olefinic C-H bond functionalization/cyclization cascade reaction followed by rearomatization led to the desired molecules in one step under mild reaction conditions. This protocol also displays a broad substrate scope and good tolerance to a wide range of functional groups. Additionally, the potential utility for the synthesis of highly conjugated polybenzenes and diversification of natural products was also demonstrated.
