133073-81-1 Usage
Uses
Used in Fragrance Industry:
1-tert-butyl-3-ethoxybenzene is used as a fragrance ingredient for its sweet odor, contributing to the production of perfumes and other fragrance products.
Used in Solvent Applications:
1-tert-butyl-3-ethoxybenzene is used as a solvent for various substances due to its ability to dissolve a wide range of materials, making it useful in various industrial processes.
Used in Antioxidant and Antibacterial Applications:
1-tert-butyl-3-ethoxybenzene has been found to possess potential antioxidant and antibacterial properties, which can be utilized in different applications where these properties are beneficial.
However, it is important to note that exposure to 1-tert-butyl-3-ethoxybenzene can cause irritation to the skin, eyes, and respiratory system, and prolonged or repeated exposure may lead to adverse health effects. Therefore, proper handling, storage, and safety measures are crucial to minimize potential risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 133073-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,7 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133073-81:
(8*1)+(7*3)+(6*3)+(5*0)+(4*7)+(3*3)+(2*8)+(1*1)=101
101 % 10 = 1
So 133073-81-1 is a valid CAS Registry Number.
133073-81-1Relevant articles and documents
Synthesis of m-Alkylphenols via a Ruthenium-Catalyzed C-H Bond Functionalization of Phenol Derivatives
Li, Gang,Gao, Panpan,Lv, Xulu,Qu, Chen,Yan, Qingkai,Wang, Ya,Yang, Suling,Wang, Junjie
, p. 2682 - 2685 (2017)
The first example of the synthesis of m-alkylphenols via a ruthenium-catalyzed CAr-H bond functionalization of phenol derivatives with sec/tert-alkyl bromides is reported. Mechanistic studies indicated that the m-CAr-H bond alkylation may involve a radical process and that a six-membered ruthenacycle complex was the active catalyst. Moreover, this approach can provide an expedited strategy for the atom-/step-economical synthesis of many noteworthy pharmaceuticals and other functional molecules.
