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Allyl 4-(trifluoromethyl)benzoate is an organic compound with the chemical formula C11H9F3O2. It is a colorless to pale yellow liquid with a fruity, floral, and green odor. allyl 4-(trifluoromethyl)benzoate is primarily used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions, due to its pleasant scent. It is also employed as a flavoring agent in food and beverages, imparting a fruity and floral taste. The compound is synthesized through the esterification of allyl alcohol with 4-(trifluoromethyl)benzoic acid, and it is considered to be relatively stable and non-toxic. However, it is essential to handle it with care, as it may cause skin and eye irritation, and prolonged exposure may lead to respiratory issues.

329-81-7

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329-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329-81-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 329-81:
(5*3)+(4*2)+(3*9)+(2*8)+(1*1)=67
67 % 10 = 7
So 329-81-7 is a valid CAS Registry Number.

329-81-7Relevant academic research and scientific papers

Mechanistic studies on the nickel-catalyzed polymerization of isocyanides

Deming, Timothy J.,Novak, Bruce M.

, p. 9101 - 9111 (1993)

All mechanistic aspects of nickel-mediated isocyanide polymerizations have been examined experimentally. Chain initiation has been studied by 13C{1H} NMR at low temperature using a living polymerization system. Chain propagation has been examined by cyclic voltammetry, ESR spectroscopy, magnetic susceptibility measurements, temperature dependent kinetic studies, and substituent effect analysis. The chain-propagation studies were performed on both living and classical heterogeneous systems and were found to be invariant with respect to the type of nickel initiator used. Finally, chain-transfer reactions were studied by NMR, kinetic studies, substituent effect analyses, and chemical studies. Comprehensive mechanistic schemes have been derived from the experimental data and are presented as the most probable reaction pathways.

Toluates: unexpectedly versatile reagents

Lam, Kevin,Markó, István E.

supporting information; experimental part, p. 10930 - 10940 (2010/02/28)

The mechanism of the monoelectronic reduction of aromatic esters has been investigated. The unexpected synthetic utility of the toluate moiety in the deoxygenation of alcohols and the allylation of ketones is also reported. Finally, the use of aromatic esters as robust, though easily removable, protecting groups is depicted.

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