4419-58-3 Usage
Physical state
Clear, colorless liquid the compound appears as a transparent liquid without any color, which facilitates its usage in various applications.
Odor
Faint the compound has a very subtle smell, making it less intrusive in industrial and commercial settings.
Usage as a solvent
Commonly used 1-tert-Butyloxy-3,3-dimethylbutane is often employed as a solvent to dissolve and mix with other substances in chemical processes.
Usage as an intermediate
In the production of other chemicals the compound serves as a starting material or building block in the synthesis of other chemical compounds.
Pharmaceutical manufacturing
Used in the production of pharmaceuticals the compound is utilized in the creation of various medications and healthcare products.
Low acute toxicity
Relatively safe for industrial and commercial applications 1-tert-Butyloxy-3,3-dimethylbutane has a low level of toxicity, making it suitable for use in a wide range of settings.
Proper handling and storage
Essential for minimizing potential risks to ensure the safe use of 1-tert-Butyloxy-3,3-dimethylbutane, it is crucial to follow appropriate handling and storage procedures as recommended by safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 4419-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4419-58:
(6*4)+(5*4)+(4*1)+(3*9)+(2*5)+(1*8)=93
93 % 10 = 3
So 4419-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O/c1-9(2,3)7-8-11-10(4,5)6/h7-8H2,1-6H3
4419-58-3Relevant articles and documents
Solvomercuration-Demercuration. 11. Alkoxymercuration-Demercuration of Representative Alkenes in Alcohol Solvents with the Mercuric Salts Acetate, Trifluoroacetate, Nitrate, and Methanesulfonate
Brown, Herbert C.,Kurek, Joseph T.,Rei, Min-Hon,Thompson, Kerry L.
, p. 2551 - 2557 (2007/10/02)
The alkoxymercuration-demercuration of seven representative olefins with the mercuric salts acetate, trifluoroacetate, nitrate, and methanesulfonate, in methyl, ethyl, isopropyl, and tert-butyl alcohols was examined.Mercuric acetate was effective only in methanol and ethanol.On the other hand, mercuric trifluoroacetate was effective in all four solvents, giving in most cases high yields of the corresponding ethers.Both mercuric nitrate and mercuric methanesulfonate were effective in methanol, ethanol, and 2-propanol.However, in several cases poor selectivity for the ether was observed, as evidenced by the formation of significant amounts of side products.Both electronic and steric effects are important factors in the reaction.Moreover, the structure of the olefin has a pronounced effect, both on the types of oxymercurials formed and on their stability to the reaction conditions.
