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Ethanone,1-[5-(5-chloro-2-hydroxyphenyl)-2-thienyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71866-91-6

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71866-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71866-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71866-91:
(7*7)+(6*1)+(5*8)+(4*6)+(3*6)+(2*9)+(1*1)=156
156 % 10 = 6
So 71866-91-6 is a valid CAS Registry Number.

71866-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[5-(5-chloro-2-hydroxyphenyl)thiophen-2-yl]ethanone

1.2 Other means of identification

Product number -
Other names 2-<5-acetyl thien-2-yl>-4-chlorophenol

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:71866-91-6 SDS

71866-91-6Downstream Products

71866-91-6Relevant academic research and scientific papers

Iron(III)-Catalyzed Chlorination of Activated Arenes

Mostafa, Mohamed A. B.,Bowley, Rosalind M.,Racys, Daugirdas T.,Henry, Martyn C.,Sutherland, Andrew

, p. 7529 - 7537 (2017/07/26)

A general and regioselective method for the chlorination of activated arenes has been developed. The transformation uses iron(III) triflimide as a powerful Lewis acid for the activation of N-chlorosuccinimide and the subsequent chlorination of a wide range of anisole, aniline, acetanilide, and phenol derivatives. The reaction was utilized for the late-stage mono- and dichlorination of a range of target compounds such as the natural product nitrofungin, the antibacterial agent chloroxylenol, and the herbicide chloroxynil. The facile nature of this transformation was demonstrated with the development of one-pot, tandem, iron-catalyzed dihalogenation processes allowing highly regioselective formation of different carbon-halogen bonds. The synthetic utility of the resulting dihalogenated aryl compounds as building blocks was established with the synthesis of natural products and pharmaceutically relevant targets.

STRUCTURE AND SYNTHESIS OF CHLOROPHENOL DERIVATIVES FROM HELICHRYSUM SPECIES

Bohlmann, Ferdinand,Knauf, Werner,Misra, Laxmi N.

, p. 4987 - 4990 (2007/10/02)

The isolation of a further chlorophenol acetylene from Helichrysum coriaceum as well as the synthesis of three naturally occuring chlorophenols are described.

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