21926-53-4 Usage
Uses
Used in Pesticide Industry:
Methyl [4-(chlorosulfonyl)phenyl]carbamate serves as an active ingredient in pesticides, leveraging its ability to inhibit cholinesterase for controlling a variety of insect pests. Its application aims to protect crops from damage caused by insects, thereby ensuring agricultural productivity.
Used in Insecticide Formulations:
In the realm of insecticides, Methyl [4-(chlorosulfonyl)phenyl]carbamate is utilized as a key component in formulations designed to combat insect infestations. It targets the nervous systems of insects, disrupting their normal functioning and leading to their death, which is beneficial for curbing the spread of insect-borne diseases and protecting stored products from infestation.
Given the potential toxicity and environmental impact of Methyl [4-(chlorosulfonyl)phenyl]carbamate, its application in these industries is subject to stringent regulations in many countries to mitigate risks to human health and ecological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 21926-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,2 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21926-53:
(7*2)+(6*1)+(5*9)+(4*2)+(3*6)+(2*5)+(1*3)=104
104 % 10 = 4
So 21926-53-4 is a valid CAS Registry Number.
21926-53-4Relevant academic research and scientific papers
Active compound for inhibiting intestinal inflammation reaction
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Paragraph 0074-0077, (2021/10/27)
The structure is shown in the formula I, and the definition of each substituent is as described in the specification and claims. The compound can promote intestinal mucosal repair and barrier homeostasis maintenance, thereby inhibiting over-activated inte
(4-Arylsulfamoyl)phenylcarbamic acid esters: I. Synthesis and activity against herpes viruses
Krutikov,Erkin,Tets,Shmarov
, p. 1567 - 1573 (2016/08/26)
Aiming to modify the biological activity of sulfonamides, a number of alkyl (4-arylsulfamoyl)- phenylcarbamates were prepared in 50–70% yield. Biological screening showed that the target compounds possessed a high activity against herpes viruses as well as a traditional antibiotic one.
