336880-01-4 Usage
General Description
2-[(2-chloro-6-fluorobenzyl)oxy]benzaldehyde is a chemical compound with the molecular formula C14H10ClFO2. It is a benzaldehyde derivative with a benzene ring substituted by a chloro and a fluorine atom, as well as an oxy group attached to a benzyl group. 2-[(2-CHLORO-6-FLUOROBENZYL)OXY]BENZALDEHYDE has potential applications in pharmaceuticals and organic synthesis, and it may be used as an intermediate in the production of various organic compounds. Additionally, it has been studied for its potential biological activities and pharmacological properties. However, it is important to handle this chemical with caution due to its potential hazards and to follow appropriate safety measures and guidelines when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 336880-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,8,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 336880-01:
(8*3)+(7*3)+(6*6)+(5*8)+(4*8)+(3*0)+(2*0)+(1*1)=154
154 % 10 = 4
So 336880-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClFO2/c15-12-5-3-6-13(16)11(12)9-18-14-7-2-1-4-10(14)8-17/h1-8H,9H2
336880-01-4Relevant articles and documents
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)
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.
