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"Lithium, [3-(trifluoromethyl)phenyl]-" is a chemical compound with the molecular formula C7H4F3Li. It is an organometallic compound, which means it contains a carbon-metal bond, in this case, between lithium and the phenyl group. The compound features a phenyl ring (a six-carbon aromatic ring) with a trifluoromethyl group (CF3) attached at the 3-position. This trifluoromethyl group imparts unique electronic and steric properties to the molecule, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is often used in organic synthesis as a nucleophile or a reducing agent.

368-49-0

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368-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 368-49-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 368-49:
(5*3)+(4*6)+(3*8)+(2*4)+(1*9)=80
80 % 10 = 0
So 368-49-0 is a valid CAS Registry Number.

368-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name lithium,trifluoromethylbenzene

1.2 Other means of identification

Product number -
Other names m-trifluoromethylphenyl lithium

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:368-49-0 SDS

368-49-0Relevant academic research and scientific papers

Relative basicities of ortho-, meta-, and para-substituted aryllithiums

Gorecka-Kobylinska, Joanna,Schlosser, Manfred

experimental part, p. 222 - 229 (2009/04/11)

(Chemical Equation Presented) The relative basicities of aryllithiums bearing methoxy, chlorine, fluorine, trifluoromethyl and trifluoromethoxy substituents at the ortho, meta, and para positions have been assessed. To this end, two aryllithiums of compar

Method for producing, via organometallic compounds, organic intermediate products

-

Page/Page column 4, (2008/06/13)

The present invention provides a process for preparing aryllithium compounds by reacting haloaliphatics with lithium metal to form a lithium alkyl and reacting the lithium alkyl with aromatic halogen compounds of formula (III) in a halogen-metal exchange reaction to form the corresponding lithium aromatics of formula (IV).

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