75465-42-8 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from 1,2,4-Thiadiazol-5-ol by forming an ester bond with a methylcarbamate group.
Explanation
The CAS (Chemical Abstracts Service) number is a unique identifier assigned to a specific chemical compound.
Explanation
The compound has potential uses in these industries due to its insecticidal and acaricidal properties.
Explanation
The compound has the ability to kill insects, making it useful for controlling pests in agriculture.
Explanation
The compound is effective in controlling mite and tick populations, which can be beneficial in both agricultural and medical contexts.
Explanation
Due to its potential toxicity, it is important to handle this chemical compound with caution to minimize health risks.
Explanation
The compound's properties make it a candidate for use in multiple applications, including pharmaceuticals and agriculture, but it should be used responsibly.
Ester derivative
1,2,4-Thiadiazol-5-ol
Potential applications
Pharmaceutical and agricultural industries
Insecticidal properties
Kills insects
Acaricidal properties
Kills mites and ticks
Health risks
Handle with care
Versatile chemical
Potential uses in various fields
Check Digit Verification of cas no
The CAS Registry Mumber 75465-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,6 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75465-42:
(7*7)+(6*5)+(5*4)+(4*6)+(3*5)+(2*4)+(1*2)=148
148 % 10 = 8
So 75465-42-8 is a valid CAS Registry Number.
75465-42-8Relevant academic research and scientific papers
Action des isocyanates sur les bezisothiazol-2,1 ones-3(1H9 et sur les thiadiazol-1,2,4 ones-5: un nouveau rearrangement avec extrusion del'atome de soufre
Perronnett, Jacques,Taliani, Laurent
, p. 673 - 678 (2007/10/02)
The reaction of isocyanates with 2,1-bezisothiazol-3-(1H)ones and on 1,2,4-thiadiazol-5-(4H)ones was investigated.With a stoichiometric amount of organic base the reaction resulted, in both cases, in the incorporation of two atoms of the isocyanate into t
