56046-17-4 Usage
Description
1-(4-ISOPROPYLPHENYL)UREA, also known as a phenylurea fungicide, is a chemical compound belonging to the class of ureas. It is characterized by the substitution of a p-cumenyl group at the 1-position and is a metabolite of the herbicide isoproturon. 1-(4-ISOPROPYLPHENYL)UREA exhibits fungicidal properties, making it a valuable component in the agricultural industry.
Uses
Used in Agricultural Industry:
1-(4-ISOPROPYLPHENYL)UREA is used as a fungicide for protecting wheat, grains, and vegetable crops from fungal infections. Its application helps to maintain crop health and yield, ensuring a stable food supply.
As a Pesticide Component:
In addition to its direct application as a fungicide, 1-(4-ISOPROPYLPHENYL)UREA is also utilized as a component in the formulation of various pesticides. Its inclusion in these products enhances their overall effectiveness in controlling pests and diseases, contributing to improved agricultural productivity and crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 56046-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,4 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56046-17:
(7*5)+(6*6)+(5*0)+(4*4)+(3*6)+(2*1)+(1*7)=114
114 % 10 = 4
So 56046-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O/c1-7(2)8-3-5-9(6-4-8)12-10(11)13/h3-7H,1-2H3,(H3,11,12,13)
56046-17-4Relevant articles and documents
Direct conversion of carboxylic acids to various nitrogen-containing compounds in the one-pot exploiting curtius rearrangement
Kumar, Arun,Kumar, Naveen,Sharma, Ritika,Bhargava, Gaurav,Mahajan, Dinesh
, p. 11323 - 11334 (2019/09/10)
Herein we report, a single-pot multistep conversion of inactivated carboxylic acids to various N-containing compounds using a common synthetic methodology. The developed methodology rendered the use of carboxylic acids as a direct surrogate of primary amines, for the synthesis of primary ureas, secondary/tertiary ureas, O/S-carbamates, benzoyl ureas, amides, and N-formyls, exploiting the Curtius reaction. This approach has a potential to provide a diversified library of N-containing compounds, starting from a single carboxylic acid, based on the selection of the nucleophile.