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Benzamide, N,N-diethyl-2,3,4,5,6-pentafluoro- is a chemical compound with the molecular formula C9H10F5NO. It is a derivative of benzamide, featuring a pentafluorophenyl group attached to the amide nitrogen. Benzamide, N,N-diethyl-2,3,4,5,6-pentafluoro- is characterized by its unique electronic properties due to the presence of five fluorine atoms on the phenyl ring, which can significantly influence its reactivity and stability. It is used in various chemical reactions and synthesis processes, particularly in the field of pharmaceuticals and materials science, where its fluorinated structure can impart specific properties to the final products. The compound is also of interest in research for its potential applications in the development of new drugs and advanced materials.

889-98-5

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889-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 889-98-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 889-98:
(5*8)+(4*8)+(3*9)+(2*9)+(1*8)=125
125 % 10 = 5
So 889-98-5 is a valid CAS Registry Number.

889-98-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethyl-2,3,4,5,6-pentafluorobenzamide

1.2 Other means of identification

Product number -
Other names N.N-Diaethyl-pentafluorbenzamid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:889-98-5 SDS

889-98-5Relevant academic research and scientific papers

Copper-Catalyzed Defluorinative Hydroarylation of Alkenes with Polyfluoroarenes

Fu, Bin,Li, Xiaohong,Xiong, Tao,Yuan, Xiuping,Zhang, Qian,Zhang, Qiao

supporting information, p. 23056 - 23060 (2020/10/19)

A catalytic defluorinative hydroarylation of alkenes with polyfluoroarenes in the presence of dppbz-ligated Cu catalyst and silanes was developed. This method provides a straightforward and alternative avenue to synthetic important polyfluorinated arenes with readily available and bench-stable alkenes as latent nucleophiles, and therefore avoids conventional reliance on stoichiometric quantities of organometallic reagents. This reaction proceeds under very mild conditions and exhibits good functional group compatibility and high level of regioselectivity. The synthetic potential of this method was further demonstrated by a gram-scale synthesis, and an array of experimental studies were also carried out to elaborate the probable mechanism.

Multicomponent Coupling Reaction of Perfluoroarenes with 1,3-Butadiene and Aryl Grignard Reagents Promoted by an Anionic Ni(II) Complex

Iwasaki, Takanori,Fukuoka, Asuka,Min, Xin,Yokoyama, Wataru,Kuniyasu, Hitoshi,Kambe, Nobuaki

supporting information, p. 4868 - 4871 (2016/10/18)

An anionic Ni complex was isolated and its structure determined by X-ray crystallography. With such an anionic complex as a key intermediate, a regio- and stereoselective multicomponent coupling reaction of perfluoroarenes, aryl Grignard reagents, and 1,3-butadiene in a 1:1:2 ratio was achieved, resulting in the formation of 1,6-octadiene derivatives containing two aryl groups, one from the perfluoroarene and the other from the aryl Grignard reagent, at the 3- and 8-positions, respectively.

Palladium-catalyzed coupling of polyfluorinated arenes with heteroarenes via C-F/C-H activation

Yu, Daohong,Lu, Long,Shen, Qilong

supporting information, p. 940 - 943 (2013/03/29)

The first palladium-catalyzed coupling of 2-pyridyl-polyfluoroarenes and benzoxazole, thiazole, benzothiazole, benzoimidazole, oxazole or oxadiazole via a concurrent C-F/C-H activation is described. Initial mechanistic studies showed that C-F activation o

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