154825-26-0 Usage
Urea group
Central feature of the compound
Urea group
Contains two amine (-NH2) groups bonded to a carbonyl group (C=O)
Furan moiety
A five-membered ring with four carbon atoms and one oxygen atom, bonded to the urea group
Nitrophenyl group
A phenyl group (a six-membered ring with six carbon atoms) with a nitro group (-NO2) attached, bonded to the urea group
Furan ring
Aromatic ring with a single oxygen atom
Nitro group
A functional group with the structure -NO2
Pharmaceuticals
Due to its diverse structural features, it may have potential as a drug molecule or a building block for drug development
Agricultural chemicals
Its structural properties may make it useful in the development of new pesticides or other agrochemicals
Materials science
The compound's unique structure could be utilized in the development of new materials with specific properties
Research needs
Further research is required to fully understand the properties and potential applications of 1-(furan-2-ylmethyl)-3-(4-nitrophenyl)urea, as its diverse structural features may lead to a wide range of uses in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 154825-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,8,2 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 154825-26:
(8*1)+(7*5)+(6*4)+(5*8)+(4*2)+(3*5)+(2*2)+(1*6)=140
140 % 10 = 0
So 154825-26-0 is a valid CAS Registry Number.
154825-26-0Relevant articles and documents
Photocatalyzed synthesis of unsymmetrical ureas via the oxidative decarboxylation of oxamic acids with PANI-g-C3N4-TiO2 composite under visible light
Wang, Liang,Wang, Hao,Wang, Yaoyao,Shen, Minggui,Li, Shubai
supporting information, (2020/04/28)
The synthesis of unsymmetrical ureas via the photocatalyzed oxidative decarboxylation of oxamic acids has been developed. The carbamoyl radicals were generated from oxamic acids in the presence of a hypervalent iodine reagent and the PANI(Polyaniline)-g-C3N4-TiO2 composite under visible light irradiation. The radicals were converted in situ into the corresponding isocyanates, which were then trapped by amines to afford the corresponding products in moderate to good yields. This protocol avoided the direct use of environmentally unfriendly isocyanates and a series of substrates were tolerated. Moreover, the photocatalyst could be readily recovered by simple filtration and be reused for several runs with only a slight decrease in the catalytic activity.
