5658-46-8 Usage
Description
[(2-methylprop-2-en-1-yl)oxy]methylbenzene, also known as isobutylbenzene, is a colorless liquid with a strong odor and a molecular formula of C11H16O. It is a compound commonly used in various industrial applications due to its versatile properties.
Uses
Used in Paints and Coatings Industry:
[(2-methylprop-2-en-1-yl)oxy]methylbenzene is used as a solvent for its ability to dissolve a wide range of substances, which is crucial in the formulation of paints and coatings to achieve desired properties such as adhesion, durability, and appearance.
Used in Adhesives Industry:
In the adhesives industry, [(2-methylprop-2-en-1-yl)oxy]methylbenzene is used as a solvent to enhance the adhesive's bonding capabilities and improve its performance on various substrates.
Used in Chemical Production:
[(2-methylprop-2-en-1-yl)oxy]methylbenzene is utilized as an intermediate in the production of other chemicals, contributing to its versatility and importance in the chemical industry.
Used in Fragrance Industry:
As a fragrance ingredient, [(2-methylprop-2-en-1-yl)oxy]methylbenzene is used in perfumes and personal care products to provide a unique and strong scent.
Used in Pharmaceutical and Agrochemical Synthesis:
[(2-methylprop-2-en-1-yl)oxy]methylbenzene serves as a precursor in the synthesis of various pharmaceuticals and agrochemicals, highlighting its role in these critical industries.
Safety Precautions:
It is important to handle [(2-methylprop-2-en-1-yl)oxy]methylbenzene with care, as it is flammable and can cause irritation to the skin, eyes, and respiratory system upon exposure. Proper safety measures should be taken to minimize risks during its use and handling.
Check Digit Verification of cas no
The CAS Registry Mumber 5658-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5658-46:
(6*5)+(5*6)+(4*5)+(3*8)+(2*4)+(1*6)=118
118 % 10 = 8
So 5658-46-8 is a valid CAS Registry Number.
5658-46-8Relevant articles and documents
Contra-Thermodynamic Positional Isomerization of Olefins
Zhao, Kuo,Knowles, Robert R.
supporting information, p. 137 - 144 (2022/01/19)
A light-driven method for the contra-thermodynamic positional isomerization of olefins is described. In this work, stepwise PCET activation of a more substituted and more thermodynamically stable olefin substrate is mediated by an excited-state oxidant an
Synthesis of Piperidine Derivatives by Rhodium- Catalyzed Tandem Reaction of N-Sulfonyl-1,2,3-Triazole and Vinyl Ether
Yu, Sisi,An, Yuehui,Wang, Wenlin,Xu, Ze-Feng,Li, Chuan-Ying
supporting information, p. 2125 - 2130 (2018/04/17)
A chemoselective tandem reaction of 4-acyloxymethylene-1-sulfonyl-1,2,3-triazole and vinyl ether was reported, producing polysubstituted piperidine derivatives in up to 96% yield. The key intermediate N-sulfonyl 1-azadiene generated by migration of the OAc group to the α-imino rhodium carbene was isolated and a plausible mechanism was proposed. Several related ring systems were constructed from the highly functionalized products. (Figure presented.).
Brook Rearrangement as Trigger for Carbene Generation: Synthesis of Stereodefined and Fully Substituted Cyclobutenes
Zhang, Fa-Guang,Marek, Ilan
supporting information, p. 8364 - 8370 (2017/06/28)
Through a sequence that can be performed in a single vessel, involving regio- and diastereoselective copper-catalyzed carbomagnesiation of cyclopropenes, reaction with acylsilanes, and addition of THF as cosolvent, Brook rearrangement can be triggered to furnish a wide range of cyclobutenes with exceptional diastereoselectivity. Accordingly, stereodefined and highly substituted cyclobutenes with contiguous quaternary carbon centers can be synthesized easily and in high yield. The new strategy constitutes an unprecedented application of Brook rearrangement, one which involves the intermediacy of carbene species.
