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41177-03-1

(4-methyl-cyclohexyl)-carbamic acid methyl ester, also known as 4-methylcyclohexylmethylcarbamate or Meobal, is an organocarbamate compound with the chemical formula C9H17NO2. It is a colorless to pale yellow liquid with a mild, fruity odor. This chemical is primarily used as an insecticide, particularly for the control of various pests in agriculture, such as aphids, mites, and whiteflies. It works by inhibiting the acetylcholinesterase enzyme in the nervous system of insects, leading to their paralysis and eventual death. Meobal is known for its broad-spectrum activity and relatively low mammalian toxicity, making it a popular choice for integrated pest management strategies. However, it is important to follow proper application guidelines and safety measures to minimize potential risks to non-target organisms and the environment.

41177-03-1

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41177-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41177-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,7 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41177-03:
(7*4)+(6*1)+(5*1)+(4*7)+(3*7)+(2*0)+(1*3)=91
91 % 10 = 1
So 41177-03-1 is a valid CAS Registry Number.

41177-03-1Downstream Products

41177-03-1Relevant articles and documents

Ruthenium-Na2CO3-catalyzed one-pot synthesis of ring-hydrogenated carbamates from aromatic amines and organic carbonates under H2

Cho, Jin Ku,Kim, Hoon Sik,Kim, Yong Jin,Mishra, Vivek,Shin, Seung-Han,Suh, Young-Woong

, p. 82 - 90 (2014)

A facile and efficient one-pot procedure for the synthesis of ring hydrogenated carbamates from aromatic amine and alkylene carbonate under H2 gas pressure has been developed using a heterogeneous catalyst system comprising ruthenium and alkali metal carbonates. The effects of temperature, H2 pressure, catalyst (types of loaded metal and their supports), molar ratio of substrate/catalyst, and solvent were also investigated. Among the alkali metal carbonates, the sodium carbonate was found as best promoter for nucleophilic attack and ring-opening (NARO) reaction and thus increased the yield of ring hydrogenated carbamate up to 88% when using Ru/C as ring hydrogenation (RH) catalyst. This catalyst system could be reused at least five times without signi?cant loss of activity, which makes this process cost-effective and eco-friendly.

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