79069-41-3 Usage
Uses
Used in Chemical Industry:
Benzenamine, 2,4-bis(1-methylethyl)is used as a solvent for various chemical reactions and processes. Its ability to dissolve a wide range of substances makes it a versatile component in the chemical industry.
Used in Pharmaceutical Industry:
Diisopropylbenzene is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique chemical structure allows it to be a key component in the production of certain drugs.
Used in Research and Development:
Benzenamine, 2,4-bis(1-methylethyl)is utilized in research and development for the study of chemical reactions and the development of new compounds. Its properties make it a valuable tool for scientists and researchers in various fields.
Used in Laboratory Settings:
Diisopropylbenzene is used in laboratory settings for various experiments and analyses. Its solubility and reactivity make it a useful substance for testing and studying different chemical reactions.
Used in Industrial Cleaning:
Benzenamine, 2,4-bis(1-methylethyl)is used in industrial cleaning processes to remove grease, oil, and other contaminants from surfaces. Its solvent properties make it effective in breaking down and removing these substances.
Used in Manufacturing Processes:
Diisopropylbenzene is used in manufacturing processes as a component in the production of various products, such as plastics, rubber, and coatings. Its versatility as a solvent and its ability to dissolve a wide range of substances make it a valuable asset in these industries.
Used in Quality Control:
Benzenamine, 2,4-bis(1-methylethyl)is used in quality control to ensure the purity and consistency of products in various industries. Its ability to dissolve substances and its reactivity make it a useful tool for testing and analyzing the quality of products.
Used in Environmental Applications:
Diisopropylbenzene is used in environmental applications to help break down and remove contaminants from soil and water. Its solvent properties make it effective in degrading and eliminating pollutants.
Used in Safety and Emergency Response:
Benzenamine, 2,4-bis(1-methylethyl)is used in safety and emergency response situations to help control and mitigate chemical spills and leaks. Its ability to dissolve substances and its reactivity make it a valuable tool in these scenarios.
Check Digit Verification of cas no
The CAS Registry Mumber 79069-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,6 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79069-41:
(7*7)+(6*9)+(5*0)+(4*6)+(3*9)+(2*4)+(1*1)=163
163 % 10 = 3
So 79069-41-3 is a valid CAS Registry Number.
79069-41-3Relevant academic research and scientific papers
Electrochemical Amination of Less-Activated Alkylated Arenes Using Boron-Doped Diamond Anodes
Herold, Sebastian,M?hle, Sabine,Zirbes, Michael,Richter, Frank,Nefzger, Hartmut,Waldvogel, Siegfried R.
supporting information, p. 1274 - 1278 (2016/03/19)
The anodic C-H amination of aromatic compounds is a powerful and versatile method for the synthesis of aniline derivatives. By using boron-doped diamond (BDD) anodes, a method initially described by Yoshida et al. for electron-rich arenes was expanded to less-activated aromatic systems e.g., simple alkylated benzene derivatives. Anodes based on sp3 carbon seem to be the key for the electrochemical amination reaction. The corresponding primary anilines are obtained in good yields. Despite the cationic intermediates of the electrolytic reaction tert-butyl moieties are tolerated.
5-[PHENYL-TETRAHYDRONAPHTHALENE-2-YL DIHYDRONAPHTHALEN-2-YL AND HETEROARYL-CYCLOPROPYL]-PENTADIENOIC ACID DERIVATIVES HAVING SERUM GLUCOSE REDUCING ACTIVITY
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Page 30, (2010/02/10)
Compounds of the formula where the variables have the meaning defined in the specification are capable of reducing serum glucose levels in diabetic mammals without the undesirable side effects of reducing serum thyroxine levels and transiently increasing triglyceride levels.
