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124004-74-6

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124004-74-6 Usage

General Description

2,2,2-trifluoro-1-(2-fluorophenyl)ethanol is a chemical compound with the molecular formula C8H6F4O. It is a colorless liquid that is used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. 2,2,2-trifluoro-1-(2-fluorophenyl)ethanol contains a trifluoromethyl group attached to a benzene ring and an ethanol group, making it a versatile building block for the synthesis of various organic compounds. It is commonly used as a reagent in organic synthesis reactions and as a building block for the preparation of fluorinated compounds. Additionally, it has potential applications in the field of medicinal chemistry due to its unique structural features and fluorine substituents. Overall, 2,2,2-trifluoro-1-(2-fluorophenyl)ethanol is an important chemical with diverse applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 124004-74-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,0 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124004-74:
(8*1)+(7*2)+(6*4)+(5*0)+(4*0)+(3*4)+(2*7)+(1*4)=76
76 % 10 = 6
So 124004-74-6 is a valid CAS Registry Number.

124004-74-6SDS

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 2,2,2-trifluoro-1-(2-fluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2,2,2-trifluoro-1-(2'-fluorophenyl)ethanol

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:124004-74-6 SDS

124004-74-6Relevant articles and documents

Asymmetric Hydrogenation of Aryl Perfluoroalkyl Ketones Catalyzed by Rhodium(III) Monohydride Complexes Bearing Josiphos Ligands

Brüning, Fabian,Nagae, Haruki,K?ch, Daniel,Mashima, Kazushi,Togni, Antonio

supporting information, p. 10818 - 10822 (2019/07/31)

The asymmetric hydrogenation of 2,2,2-trifluoroacetophenones and aryl perfluoroalkyl ketones was developed using a unique, well-defined chloride-bridged dinuclear rhodium(III) complex bearing Josiphos-type diphosphine ligands. These complexes were prepared from [RhCl(cod)]2, Josiphos ligands, and hydrochloric acid. As catalyst precursors, they allow for the efficient and enantioselective synthesis (up to 99 % ee) of chiral secondary alcohols with perfluoroalkyl groups. This system does not require an activating base for the hydrogenation of 2,2,2-trifluoroacetophenones. Additionally, the enantioselective C=O hydrogenations of 2-phenyl-3-(haloacetyl)-indoles, a class of privileged structures in medicinal chemistry, is reported for the first time.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Paragraph 0140; 0156; 0157, (2015/12/30)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula (“Formula One”).

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Paragraph 0654-0655, (2014/06/25)

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

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