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Benzene, 1-methyl-3-(phenoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19962-22-2

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19962-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19962-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19962-22:
(7*1)+(6*9)+(5*9)+(4*6)+(3*2)+(2*2)+(1*2)=142
142 % 10 = 2
So 19962-22-2 is a valid CAS Registry Number.

19962-22-2Downstream Products

19962-22-2Relevant academic research and scientific papers

Choline Hydroxide as a Versatile Medium for Catalyst-Free O-Functionalization of Phenols

Joo, Seong-Ryu,Kim, Seung-Hoi,Kwon, Gyu-Tae,Park, Soo-Youl

, p. 1200 - 1205 (2020/11/30)

A versatile synthetic protocol for benzyl phenyl ether preparation via O-alkylation of phenolic oxygen with readily available benzyl derivatives was demonstrated. The newly designed procedure was carried out using an eco-friendly medium, room-temperature ionic liquid (choline hydroxide), under metal- and base-catalyst-free aerobic conditions. The reaction platform was also successfully applied to phenol protection strategy.

An alternative route for boron phenoxide preparation from arylboronic acid and its application for C[sbnd]O bond formation

Joo, Seong-Ryu,Kim, Seung-Hoi,Lim, In-Kyun

, (2020/08/06)

An efficient synthetic route to benzyl phenyl ether preparation has been successfully developed via a one-pot synthetic protocol utilizing a combination of arylboronic acids, hydrogen peroxide (H2O2), and benzyl halides. The whole procedure consists of two consecutive reactions, formation of boron phenoxide from arylboronic acids and its nucleophilic attack. A simple operation under mild conditions such as room-temperature ionic liquid (choline hydroxide), aerobic environment, and absence of metal- and base-catalysts has been employed. Expansion to utilize benzyl surrogates was also successfully accomplished.

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