62487-66-5 Usage
Appearance
Yellow crystalline substance
The compound has a yellow color and forms crystals, which is a solid state with a well-defined geometric shape.
Usage
Commonly used as a pesticide
It is applied in agricultural and horticultural settings to control pests and protect crops from damage.
Acaricidal and insecticidal properties
Strong
The compound is effective in killing both insects and mites, making it a valuable tool in pest control.
Mode of action
Interfering with the nervous system of insects and mites
The compound disrupts the normal functioning of the target organisms' nervous systems, leading to their death.
Toxicity
Can be toxic to humans and non-target organisms
The compound may pose a risk to human health and other living organisms if not handled properly.
Safety precautions and handling guidelines
Essential
To minimize risks, it is crucial to follow appropriate safety measures and guidelines when working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 62487-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,8 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62487-66:
(7*6)+(6*2)+(5*4)+(4*8)+(3*7)+(2*6)+(1*6)=145
145 % 10 = 5
So 62487-66-5 is a valid CAS Registry Number.
62487-66-5Relevant academic research and scientific papers
THIOPHENES AND THEIR USE AS PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) INHIBITORS
-
Page/Page column 55, (2009/09/05)
This invention provides thiophene compounds of formula (I) : wherein R1, R2, R3, R4, n, p, and m are as described in the specification. The compounds are inhibitors of PI3K and are thus useful for treating proliferative, inflammatory, or cardiovascular disorders.
ALKYLIERUNGS- AND ARYLIERUNGSREAKTIONEN MIT GEMINALEN DITHIOLATEN
Rudorf, W. D.,Augustin, M.
, p. 329 - 336 (2007/10/02)
Acyl acetonitriles 1 react with carbon disulfide in the presence of sodium hydride to give disodium salts 2.Treatment of 2 with an alkylation reagent yields the open chain or cyclic acyl cyanketene S,S-acetals 3,4,8 and 10, respectively.Arylation to 11 is successful with 2,4-dinitro-chlorobenzene.Adding only one equivalent of methyl iodide to 2 and acidifying the reaction mixture lead to the monoalkylated compounds 7, whereas β-hydroxythioanilides 12 are available by reaction of 1 with phenyl isothiocyanate.A comparison of the ?-values shows that there exists the same type of the proton's chelation of the OH-group in 7 and 12.
