5685-47-2 Usage
Uses
Used in Chemical Synthesis:
Dicyclopropylmethane serves as a valuable building block in the synthesis of various organic compounds. Its unique structure allows it to be a key component in the creation of pharmaceuticals and agrochemicals, contributing to the development of new and improved products in these fields.
Used in Industrial Solvent Applications:
As a solvent, dicyclopropylmethane is utilized in a variety of industrial applications. Its ability to dissolve certain substances makes it a useful agent in processes that require the use of solvents to facilitate reactions or to dissolve and process materials.
Safety Considerations:
Given its volatile and flammable properties, as well as its potential to cause harm if inhaled, ingested, or if it comes into contact with the skin or eyes, dicyclopropylmethane must be handled with caution. Adequate safety measures should be implemented to minimize risks associated with its use, ensuring the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 5685-47-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5685-47:
(6*5)+(5*6)+(4*8)+(3*5)+(2*4)+(1*7)=122
122 % 10 = 2
So 5685-47-2 is a valid CAS Registry Number.
5685-47-2Relevant academic research and scientific papers
Aliphatic Azo Compounds, XV cis- and trans-Tetracyclopropyl- and Tetra-tert-butylazomethanes
Bernloehr, Werner,Flamm-ter Meer, Manuela A.,Kaiser, Juergen H.,Schmittel, Michael,Beckhaus, Hans-Dieter,Ruechardt, Christoph
, p. 1911 - 1918 (2007/10/02)
The products and the kinetics of the thermolysis of the title compounds 3 and 5 were investigated.Like the trans-isomers, the cis-azo compounds also undergo homolytic decomposition without accompanying cis-trans-isomerization.The observed structure-reactivity relationships are discussed.On irradiation of trans-tetra-tert-butylazomethane (trans-5) at 60-120 deg C in benzene or chlorobenzene an almost quantitative yield of 1,1,2,2-tetra-tert-butylethane is obtained.
