221194-62-3 Usage
Uses
Used in Solvent Applications:
(3-chloropropoxy)cyclohexane is used as a solvent in various industrial processes for its ability to dissolve a broad spectrum of substances, facilitating chemical reactions and material processing.
Used in Chemical Synthesis:
As a building block in the synthesis of other organic compounds, (3-chloropropoxy)cyclohexane is used as a starting material for creating a variety of chemical products, taking advantage of its reactivity in nucleophilic substitution, oxidation, and reduction reactions.
Used in Pharmaceutical Industry:
(3-chloropropoxy)cyclohexane is used as an intermediate in the pharmaceutical industry for the production of specific drug molecules, leveraging its chemical properties to form biologically active compounds.
Used in Environmental Applications:
Although (3-chloropropoxy)cyclohexane may pose health and environmental risks due to its potential toxicity, it is also used in the development of compounds aimed at environmental protection, such as those that help in pollution control or air and water purification.
Safety Note:
It is crucial to handle (3-chloropropoxy)cyclohexane with care due to its potential hazards. Proper safety measures should be implemented to minimize the risk of exposure and to prevent air and water pollution.
Check Digit Verification of cas no
The CAS Registry Mumber 221194-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,1,9 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 221194-62:
(8*2)+(7*2)+(6*1)+(5*1)+(4*9)+(3*4)+(2*6)+(1*2)=103
103 % 10 = 3
So 221194-62-3 is a valid CAS Registry Number.
221194-62-3Relevant academic research and scientific papers
A General Approach to Deboronative Radical Chain Reactions with Pinacol Alkylboronic Esters
André-Joyaux, Emy,Kuzovlev, Andrey,Renaud, Philippe,Tappin, Nicholas D. C.
supporting information, p. 13859 - 13864 (2020/06/10)
The generation of carbon-centered radicals from air-sensitive organoboron compounds through nucleohomolytic substitution at boron is a general method to generate non-functionalized and functionalized radicals. Due to their reduced Lewis acidity, alkylboronic pinacol esters are not suitable substrates. We report their in situ conversion into alkylboronic catechol esters by boron-transesterification with a substoichiometric amount of catechol methyl borate combined with an array of radical chain processes. This simple one-pot radical-chain deboronative method enables the conversion of pinacol boronic esters into iodides, bromides, chlorides, and thioethers. The process is also suitable the formation of nitriles and allylated compounds through C?C bond formation using sulfonyl radical traps. The power of combining radical and classical boron chemistry is illustrated with a modular 5-membered ring formation using a combination of three-component coupling and protodeboronative cyclization.
