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1-iodo-2,4,6-tris(trifluoromethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1416438-86-2

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1416438-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416438-86-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,4,3 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1416438-86:
(9*1)+(8*4)+(7*1)+(6*6)+(5*4)+(4*3)+(3*8)+(2*8)+(1*6)=162
162 % 10 = 2
So 1416438-86-2 is a valid CAS Registry Number.

1416438-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-iodo-2,4,6-tris(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:1416438-86-2 SDS

1416438-86-2Relevant academic research and scientific papers

An expedient synthesis of 2,4,6-tris(trifluoromethyl)aniline

Edelbach, Brian L.,Pharoah, Blaze M.,Bellows, Sarina M.,Thayer, Peter R.,Fennie, Charles N.,Cowley, Ryan E.,Holland, Patrick L.

, p. 3595 - 3597 (2012)

A simple two-step synthetic route leads to 2,4,6-tris(trifluoromethyl) aniline. It proceeds through deprotonation and iodination of 1,3,5-tris(trifluoromethyl)benzene, followed by copper-catalyzed amination. Georg Thieme Verlag KG Stuttgart - New York.

Catalyst-controlled aliphatic C—H oxidations

-

Page/Page column 30; 82-83; 85, (2018/04/20)

The invention provides simple small molecule, non-heme iron catalyst systems with broad substrate scope that can predictably enhance or overturn a substrate's inherent reactivity preference for sp3-hybridized C—H bond oxidation. The invention also provides methods for selective aliphatic C—H bond oxidation. Furthermore, a structure-based catalyst reactivity model is disclosed that quantitatively correlates the innate physical properties of the substrate to the site-selectivities observed as a function of the catalyst. The catalyst systems can be used in combination with oxidants such as hydrogen peroxide to effect highly selective oxidations of unactivated sp3 C—H bonds over a broad range of substrates.

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