13142-18-2 Usage
General Description
1-benzyl-3-(2,5-dichlorophenyl)urea is a chemical compound with the molecular formula C15H13Cl2N3O. It is a urea derivative with a benzyl group and two chlorophenyl groups attached to the nitrogen atom. 1-benzyl-3-(2,5-dichlorophenyl)urea is commonly used as a fungicide and insecticide in agriculture to protect crops from pests and diseases. It works by inhibiting the growth and reproduction of fungi and insects, making it an effective tool for crop protection. Additionally, it has been studied for its potential applications in medical research, particularly for its antimicrobial and antiparasitic properties. However, it is important to handle this compound with care due to its potential toxicity and environmental impacts.
Check Digit Verification of cas no
The CAS Registry Mumber 13142-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,4 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13142-18:
(7*1)+(6*3)+(5*1)+(4*4)+(3*2)+(2*1)+(1*8)=62
62 % 10 = 2
So 13142-18-2 is a valid CAS Registry Number.
13142-18-2Relevant articles and documents
Hybrid Pd/Fe3O4 nanowires: Fabrication, characterization, optical properties and application as magnetically reusable catalyst for the synthesis of N-monosubstituted ureas under ligand-free conditions
Nasrollahzadeh, Mahmoud,Azarian, Abbas,Ehsani, Ali,Sajadi, S.Mohammad,Babaei, Ferydon
, p. 168 - 175 (2014/05/20)
This paper reports the synthesis and use of Pd/Fe3O4 nanowires, as magnetically separable catalysts for ligand-free amidation coupling reactions of aryl halides with benzylurea under microwave irradiation. Then, the in situ hydrogenolysis of the products was performed to afford the N-monosubstituted ureas from good to excellent yields. This method has the advantages of high yields, simple methodology and easy work up. The catalyst can be recovered by using a magnet and reused several times without significant loss of its catalytic activity. The catalyst was characterized using the powder XRD, SEM, EDS and UV-vis spectroscopy. Experimental absorbance spectra was compared with results from the Gans theory.
