2085-66-7 Usage
Description
TERT-AMYL-TERT-BUTYLAMINE, also known as a sterically hindered secondary alkyl amine, is a chemical compound that has been investigated for its electrochemical behavior. It can be synthesized through an eco-friendly, one-pot method, making it an interesting candidate for various applications due to its unique properties.
Uses
Used in Electrochemical Applications:
TERT-AMYL-TERT-BUTYLAMINE is used as a chemical compound in electrochemical applications for its unique electrochemical behavior. Its steric hindrance and secondary alkyl amine structure make it a promising candidate for further research and development in this field.
Used in Green Synthesis:
TERT-AMYL-TERT-BUTYLAMINE is used as a key component in green synthesis processes for its eco-friendly one-pot method of production. This makes it a sustainable choice for chemical synthesis, reducing the environmental impact of its production.
Used in Chemical Research:
TERT-AMYL-TERT-BUTYLAMINE is used as a subject of study in chemical research for its unique properties and potential applications. Researchers can explore its behavior, interactions, and possible uses in various industries, contributing to the advancement of chemical science.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, TERT-AMYL-TERT-BUTYLAMINE's unique structure and properties may make it a candidate for use in the pharmaceutical industry. It could potentially be utilized in the development of new drugs or drug delivery systems, targeting specific medical conditions or therapies.
Used in Material Science:
Similarly, TERT-AMYL-TERT-BUTYLAMINE's unique properties might also find applications in material science. Its steric hindrance and electrochemical behavior could be exploited to create new materials with specific characteristics, such as improved stability or reactivity, for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2085-66-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2085-66:
(6*2)+(5*0)+(4*8)+(3*5)+(2*6)+(1*6)=77
77 % 10 = 7
So 2085-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H21N/c1-7-9(5,6)10-8(2,3)4/h10H,7H2,1-6H3
2085-66-7Relevant articles and documents
Di-tert-alkyl nitroxyl radicals. Synthesis, physical properties and applications as inhibitors of vinyl polmerization at elevated temperatures
Sosnovsky, George,Jawdosiuk, Mikolaj,Clumpner, J. Michael
, p. 109 - 126 (2007/10/03)
Stable di-tert-alkylnitroxyl radicals, tert-butyl-tert-pentylnitroxyl (4a), di-tert-pentylnitroxyl (4b) and tert-octyl-tert-pentylnitroxyl (4c), the homologs of di-tert-butylnitroxyl (1), were synthesized from tert-alkyl amines 7a-c via the 3-tert-alkylamino-3-methyl-1-butynes 8a-c. Oxidation of 8a,b with hydrogen peroxide lead to relatively unstable N-tert-alkyl-N-(1,1-dimethyl-prop-2-ynyl)nitroxyl radicals 15a,b. The thermal stability, vapor pressure data, ultraviolet, visible and electron paramagnetic resonance spectra of 4a-c were recorded. The radicals were explored as potential inhibitors of unwanted alkene polymerization reactions at elevated temperatures, in comparison with the aliphatic di-tert-butyl nitroxyl (1), the alicyclic nitroxyl radicals 2,2,6,6-tetramethylpiperidin-1-oxyl (2) and 4-hydroxy-2,2,6,6-tetramethyl-piperidin-1-oxyl (3), some commercial polymerization inhibitors, such as diethyl-hydroxylamine (Pennstop, 16), ammonium salt of N-hydroxy-N-nitrosobenzenamine (Cupferron, 17), bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate (Tinuvin 770, 18), and the well-known spin traps 2-methyl-2-nitrosopropane (19) and tert-butylhydroxylamine (20).
