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81577-11-9

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81577-11-9 Usage

General Description

1-(3-chlorophenyl)-2,2,2-trifluoroethanol is a chemical compound that consists of a trifluoroethyl group attached to a chlorophenyl group on a carbon atom, with a hydroxyl group attached to the same carbon atom. It is commonly used in organic synthesis and is a versatile building block for the preparation of various pharmaceuticals and agrochemicals. It is also used as a solvent in the pharmaceutical and manufacturing industries. The trifluoroethanol group provides strong hydrogen-bond donating properties, making it useful for promoting certain chemical reactions. Additionally, the chlorophenyl group enhances the compound's reactivity and selectivity in organic reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 81577-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81577-11:
(7*8)+(6*1)+(5*5)+(4*7)+(3*7)+(2*1)+(1*1)=139
139 % 10 = 9
So 81577-11-9 is a valid CAS Registry Number.

81577-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-2,2,2-trifluoroethanol

1.2 Other means of identification

Product number -
Other names 1-(3-chlorophenyl)-2,2,2-trifluoroethan-1-ol

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:81577-11-9 SDS

81577-11-9Relevant articles and documents

Highly enantioselective construction of CF3-bearing all-carbon quaternary stereocenters: Hiral spiro-fused bisoxazoline ligands with 1,1′-binaphthyl sidearm for asymmetric Michael-type Friedel-Crafts reaction

Bao, Robert Li-Yuan,Fu, Kang,Shi, Lei

, (2021/11/27)

A novel class of chiral spiro-fused bisoxazoline ligands possessing a deep chiral pocket was prepared. The developed ligands have been employed in the nickel-catalyzed highly enantioselective Michael-type Friedel-Crafts reaction, affording the products bearing a trifluoromethylated all-carbon quaternary stereocenter with moderate to excellent yields (up to 99%) and good to excellent enantioselectivies (up to > 99.9% ee). Moreover, a proposed model of chiral pocket revealed that the attack of indole from the Re-face of β-CF3-β-disubstituted nitroalkene was favorable.

Visible light-promoted umpolung coupling of aryl tri-/difluoroethanones with 2-alkenylpyridines

Xu, Xiao,Min, Qing-Qiang,Li, Na,Liu, Feng

supporting information, p. 11017 - 11020 (2018/10/08)

Tertiary alcohols bearing a trifluoromethyl group are of considerable medicinal interest. Using an umpolung strategy, we herein report the first intermolecular reductive cross-coupling of aryl tri-/difluoroethanones with 2-alkenylpyridines with the aid of a Br?nsted acid catalyst upon visible-light irradiation. This metal-free reaction is operationally simple and performed at ambient temperature, allowing access to desired tertiary alcohols with tri-/difluoromethyl groups in moderate to excellent yields. The commercially available and easily handled Hantzsch ester effectively serves as an electron donor, as well as a hydrogen atom source.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

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Paragraph 0141; 0165; 0166, (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”).

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