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Ethyl carbamothioylcarbamate, also known as ethyl N-(1,1-dimethylethyl)-N'-(2-oxo-1,3-thiazolidin-3-ylidene)carbamate, is a chemical compound with the molecular formula C8H14N2O2S. It is a white crystalline solid that is soluble in water and has a molecular weight of 210.28 g/mol. ethyl carbamothioylcarbamate is primarily used as an insecticide and acaricide, targeting pests such as mites, aphids, and whiteflies in agricultural settings. It works by inhibiting the synthesis of chitin, a key component in the exoskeleton of insects, leading to their death. Ethyl carbamothioylcarbamate is also known under various trade names, including Aldicarb, Temik, and Karbam. Due to its high toxicity to humans and its potential to contaminate groundwater, its use has been restricted or banned in several countries.

3673-38-9

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3673-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3673-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3673-38:
(6*3)+(5*6)+(4*7)+(3*3)+(2*3)+(1*8)=99
99 % 10 = 9
So 3673-38-9 is a valid CAS Registry Number.

3673-38-9Relevant academic research and scientific papers

Design and Synthesis of Iminosydnones for Fast Click and Release Reactions with Cycloalkynes

Riomet, Margaux,Decuypere, Elodie,Porte, Karine,Bernard, Sabrina,Plougastel, Lucie,Kolodych, Sergii,Audisio, Davide,Taran, Frédéric

supporting information, p. 8535 - 8541 (2018/05/30)

Emerging applications in the field of chemical biology are currently limited by the lack of bioorthogonal reactions allowing both removal and linkage of chemical entities on complex biomolecules. We recently discovered a novel reaction between iminosydnones and strained alkynes leading to two products resulting from ligation and fragmentation of iminosydnones under physiological conditions. We now report the synthesis of a panel of substituted iminosydnones and the structure reactivity relationship between these compounds and strained alkyne partners. This study identified the most relevant substituents, which allow to increase the rate of the transformation and to develop a bifunctional cleavable linker with improved kinetics.

Ultrashort acting hypnotic barbiturates

-

, (2008/06/13)

The subject invention concerns novel compounds that are useful as ultrashort acting hypnotic barbiturates. Specifically exemplified are derivatives of barbituric and thiobarbituric acids. They are rapidly metabolized by blood and tissue enzymes to form polar metabolites with no hypnotic activity and which are rapidly eliminated.

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