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1-(3-methylphenyl)-3-propylurea, a member of the urea class of compounds, is a white solid with the molecular formula C12H16N2O. It is recognized for its agricultural applications, particularly in controlling the growth of broadleaf weeds in various crops.

13143-27-6

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13143-27-6 Usage

Uses

Used in Agricultural Industry:
1-(3-methylphenyl)-3-propylurea is used as a herbicide for controlling the growth of broadleaf weeds in crops such as soybeans, cotton, and corn. It functions by inhibiting the production of essential proteins in weeds, thereby disrupting their growth and survival. Moreover, it is considered a relatively safe option for agricultural use, with a low potential for toxicity to humans and other non-target organisms when applied according to label instructions.

Check Digit Verification of cas no

The CAS Registry Mumber 13143-27-6 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 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13143-27:
(7*1)+(6*3)+(5*1)+(4*4)+(3*3)+(2*2)+(1*7)=66
66 % 10 = 6
So 13143-27-6 is a valid CAS Registry Number.

13143-27-6Downstream Products

13143-27-6Relevant academic research and scientific papers

A Fe3O4?SiO2/Schiff Base/Pd Complex as an Efficient Heterogeneous and Recyclable Nanocatalyst for One-Pot Domino Synthesis of Carbamates and Unsymmetrical Ureas

Inaloo, Iman Dindarloo,Majnooni, Sahar

, p. 6359 - 6368 (2019)

A palladium-catalyzed domino method for the direct synthesis of carbamates and ureas has been developed by using readily available and economical starting materials (aryl halide, carbon monoxide, sodium azide, amines and alcohols) in a one-pot approach. The domino process underwent carbonylation, Curtius rearrangement, and nucleophilic addition. This protocol provides a step-economical and highly efficient reaction to access the wide range of valuable carbamates, symmetrical and unsymmetrical ureas with high yields under remarkable mild reaction conditions that are important factors in pharmaceutical science, biochemistry and agricultural industries. Furthermore, the magnetically recoverable nanocatalyst (Fe3O4?SiO2/Pd(II)) can be conveniently and swiftly recycled using external magnet and reused at least for seven times without noticeable loss of its catalytic activity.

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