17498-71-4 Usage
Description
(2-Methyl-1-methylenepropyl)benzene, also known as isopropenyltoluene, is an aromatic hydrocarbon with the molecular formula C10H12. It is a chemical compound commonly used as a precursor for the synthesis of various industrial chemicals, including specialty polymers, resins, and coatings.
Uses
Used in Chemical Synthesis:
(2-Methyl-1-methylenepropyl)benzene is used as a precursor in the chemical synthesis of various industrial chemicals, making it an important intermediate for the production of specialty polymers, resins, and coatings.
Used in Fragrance Industry:
(2-Methyl-1-methylenepropyl)benzene is used as a fragrance ingredient in perfumes and personal care products, adding unique scents and enhancing the overall sensory experience.
Used in Fuel Additives:
(2-Methyl-1-methylenepropyl)benzene has been studied for its potential use as a fuel additive, which could improve the performance and efficiency of fuels.
Used in High-Performance Lubricants:
(2-Methyl-1-methylenepropyl)benzene is also considered for use as a component in high-performance lubricants, where it could contribute to better lubrication properties and reduced friction.
Safety Precautions:
It is important to handle (2-Methyl-1-methylenepropyl)benzene with care, as it can be harmful if ingested or inhaled and can cause irritation to the skin and eyes. Proper safety measures should be taken during its production, use, and disposal to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 17498-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,9 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17498-71:
(7*1)+(6*7)+(5*4)+(4*9)+(3*8)+(2*7)+(1*1)=144
144 % 10 = 4
So 17498-71-4 is a valid CAS Registry Number.
17498-71-4Relevant articles and documents
Chromato-mass-spectrometric identification using partition coefficients in the system of hexane-2,2,2-Trifluoroethanol
Zenkevich
, p. 1391 - 1399 (2012)
An additional characteristic of organic compounds, the partition coefficients in the heterophase solvent system n-hexane-2,2,2-trifluoroethanol, is shown to be useful for refining the results of chromatographic and gas chromatography-mass spectrometric identification. This opportunity is the most important for compounds that were not yet characterized by either mass spectra or chromatographic retention indices. Pleiades Publishing, Ltd., 2012.
Electrochemical fluorosulfonylation of styrenes
Jiang, Yi-Min,Yu, Yi,Wu, Shao-Fen,Yan, Hong,Yuan, Yaofeng,Ye, Ke-Yin
supporting information, p. 11481 - 11484 (2021/11/16)
An environmentally friendly and efficient electrochemical fluorosulfonylation of styrenes has been developed. With the use of sulfonylhydrazides and triethylamine trihydrofluoride, a diverse array of β-fluorosulfones could be readily obtained. This reaction features mild conditions and a broad substrate scope, which could also be conveniently extended to a gram-scale preparation.
Stereoselective Synthesis of Vinylcyclopropa[ b]indolines via a Rh-Migration Strategy
Guo, Pan,Sun, Wangbin,Liu, Yu,Li, Yong-Xin,Loh, Teck-Peng,Jiang, Yaojia
supporting information, p. 5978 - 5983 (2020/08/05)
A mild rhodium catalytic system has been developed to synthesize vinylcyclopropa[b]indolines through cyclopropanation of indoles with vinyl carbenoids generated from ring opening of cyclopropenes in situ. By employing a Rh-migration strategy, the products can be obtained with good to excellent E:Z ratios (≤99:1) and complete diastereoselectivity (≤99:1). This method is easy, has a low catalyst loading, and works for a broad range of functionalities.
