13208-64-5 Usage
Description
1-(4-chlorophenyl)-3-propylurea, commonly known as chlorpropham, is a chemical compound that serves as a herbicide and sprout inhibitor. It is characterized by its ability to inhibit cell division in plants, thereby preventing the growth of roots and sprouts. 1-(4-chlorophenyl)-3-propylurea is widely utilized in the agricultural industry to control weeds and promote the healthy growth of crops such as potatoes, fruits, and vegetables.
Uses
Used in Agricultural Industry:
1-(4-chlorophenyl)-3-propylurea is used as a herbicide for controlling weeds and promoting the healthy growth of crops. Its application reason lies in its ability to inhibit cell division in plants, which prevents the growth of roots and sprouts, thus reducing unwanted vegetation.
Additionally, it is used as a sprout inhibitor for potatoes, fruits, and vegetables, ensuring the quality and longevity of these produce items by preventing the sprouting process that can lead to spoilage.
However, it is important to note that there are concerns regarding the potential impact of chlorpropham on human health and the environment. It has been classified as a possible carcinogen and is toxic to aquatic organisms. Consequently, its use is heavily regulated in many countries to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 13208-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,0 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13208-64:
(7*1)+(6*3)+(5*2)+(4*0)+(3*8)+(2*6)+(1*4)=75
75 % 10 = 5
So 13208-64-5 is a valid CAS Registry Number.
13208-64-5Relevant articles and documents
Supporting-Electrolyte-Free Anodic Oxidation of Oxamic Acids into Isocyanates: An Expedient Way to Access Ureas, Carbamates, and Thiocarbamates
Petti, Alessia,Fagnan, Corentin,van Melis, Carlo G. W.,Tanbouza, Nour,Garcia, Anthony D.,Mastrodonato, Andrea,Leech, Matthew C.,Goodall, Iain C. A.,Dobbs, Adrian P.,Ollevier, Thierry,Lam, Kevin
, p. 2614 - 2621 (2021/06/27)
We report a new electrochemical supporting-electrolyte-free method for synthesizing ureas, carbamates, and thiocarbamates via the oxidation of oxamic acids. This simple, practical, and phosgene-free route includes the generation of an isocyanate intermediate in situ via anodic decarboxylation of an oxamic acid in the presence of an organic base, followed by the one-pot addition of suitable nucleophiles to afford the corresponding ureas, carbamates, and thiocarbamates. This procedure is applicable to different amines, alcohols, and thiols. Furthermore, when single-pass continuous electrochemical flow conditions were used and this reaction was run in a carbon graphite Cgr/Cgr flow cell, urea compounds could be obtained in high yields within a residence time of 6 min, unlocking access to substrates that were inaccessible under batch conditions while being easily scalable.
