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3,4,6-Trifluorophthalonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69173-87-1

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69173-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69173-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,7 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69173-87:
(7*6)+(6*9)+(5*1)+(4*7)+(3*3)+(2*8)+(1*7)=161
161 % 10 = 1
So 69173-87-1 is a valid CAS Registry Number.

69173-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,6-trifluorobenzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 3,4,6-trifluorophthalonitrile

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:69173-87-1 SDS

69173-87-1Upstream product

69173-87-1Downstream Products

69173-87-1Relevant academic research and scientific papers

Diazaphospholene-Catalyzed Hydrodefluorination of Polyfluoroarenes with Phenylsilane via Concerted Nucleophilic Aromatic Substitution

Zhang, Jingjing,Zhao, Xiao,Yang, Jin-Dong,Cheng, Jin-Pei

supporting information, p. 294 - 300 (2022/01/03)

The metal-free catalytic C-F bond activation of polyfluoroarenes was achieved with diazaphospholene as the catalyst and phenylsilane as the terminal reductant. Density functional theory calculations suggested a concerted nucleophilic aromatic substitution mechanism.

Catalyst-Free Hydrodefluorination of Perfluoroarenes with NaBH4

Schoch, Timothy D.,Mondal, Mukulesh,Weaver, Jimmie D.

supporting information, p. 1588 - 1593 (2021/03/03)

Presented is an economical means of removing fluorine from various highly fluorinated arenes using NaBH4. The procedure was adapted for different classes of perfluoroarenes. A novel isomer of an emerging class of organic dyes based on the carbazole phthalonitrile motif was succinctly synthesized in two steps from tetrafluorophthalonitrile, demonstrating the utility of the hydrodefluorination procedure. Initial exploration of the dye shows it to be photoactive and capable of facilitating contrathermodynamic styrenoid E/Z isomerization.

Transition-Metal-Free Catalytic Hydrodefluorination of Polyfluoroarenes by Concerted Nucleophilic Aromatic Substitution with a Hydrosilicate

Kikushima, Kotaro,Grellier, Mary,Ohashi, Masato,Ogoshi, Sensuke

supporting information, p. 16191 - 16196 (2017/11/27)

A transition-metal-free catalytic hydrodefluorination (HDF) reaction of polyfluoroarenes is described. The reaction involves direct hydride transfer from a hydrosilicate as the key intermediate, which is generated from a hydrosilane and a fluoride salt. The eliminated fluoride regenerates the hydrosilicate to complete the catalytic cycle. Dispersion-corrected DFT calculations indicated that the HDF reaction proceeds through a concerted nucleophilic aromatic substitution (CSNAr) process.

Hydrodefluorination of Fluoroarenes Using Hydrogen Transfer Catalysts with a Bifunctional Iridium/NH Moiety

Matsunami, Asuka,Kuwata, Shigeki,Kayaki, Yoshihito

, p. 5181 - 5185 (2016/08/18)

The hydrodefluorination of fluoroarenes with transfer hydrogenation catalysts using 2-propanol or potassium formate is described. With the aid of metal/NH cooperation, the C-N chelating Ir complexes derived from benzylic amines can efficiently promote the reduction involving the C-F bond cleavage under ambient conditions even in the absence of hydrosilanes or H2 gas, leading to the partially fluorinated products in good yields and with high selectivity.

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