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187164-20-1

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187164-20-1 Usage

Description

(S)-2-bromo-1-(2,4-dichlorophenyl)ethanol is a chiral chemical compound belonging to the class of organic compounds known as phenylpropanoids. It features a specific arrangement of atoms around its central carbon atom, which contributes to its unique properties and applications.

Uses

Used in Pharmaceutical Synthesis:
(S)-2-bromo-1-(2,4-dichlorophenyl)ethanol is used as an intermediate in the synthesis of pharmaceuticals. Its bromine and chlorine atoms facilitate diverse chemical reactions, making it a valuable component in the development of various medications.
Used in Agrochemical Production:
(S)-2-bromo-1-(2,4-dichlorophenyl)ethanol is also utilized in the production of agrochemicals, where its reactivity and structural properties are harnessed to create effective products for agricultural applications.
Used as a Reagent in Organic Synthesis:
Due to its versatility in chemical reactions, (S)-2-bromo-1-(2,4-dichlorophenyl)ethanol is often employed as a reagent in organic synthesis, contributing to the creation of a wide range of organic compounds.
Used in Antimicrobial Applications:
(S)-2-bromo-1-(2,4-dichlorophenyl)ethanol has shown potential as an antimicrobial agent. It is used to inhibit the growth of bacteria and other microorganisms, making it a useful component in the development of antibacterial products and contributing to the advancement of the antimicrobial industry.
Overall, (S)-2-bromo-1-(2,4-dichlorophenyl)ethanol is a versatile and important compound with a wide range of applications across various industries, including pharmaceuticals, agrochemicals, organic synthesis, and antimicrobial development.

Check Digit Verification of cas no

The CAS Registry Mumber 187164-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,1,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 187164-20:
(8*1)+(7*8)+(6*7)+(5*1)+(4*6)+(3*4)+(2*2)+(1*0)=151
151 % 10 = 1
So 187164-20-1 is a valid CAS Registry Number.

187164-20-1SDS

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 (1S)-2-Bromo-1-(2,4-dichlorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2,6-dichlorophenylethylamine

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:187164-20-1 SDS

187164-20-1Relevant articles and documents

COMPOUNDS OF R-(-)-(E)-[4-(2,4-DICHLOROPHENYL)-1,3-DITHIOLAN-2-YLIDENE]-1 -IMIDAZOLYLACETONITRILE-HA (LULICONAZOLE-HA) AS ANTIFUNGALS

-

Page/Page column 36, (2017/08/01)

The present invention refers to compound R-(-)-(E)-[4-(2,4-dichlorophenyl)-1,3-dithiolan-2-ylidene]-1-imidazolylacetonitrile HA, wherein HA is an acid; and to a process for their preparation. The present invention also refers to the use of compound R-(-)-(E)-[4-(2,4-dichlorophenyl)-1,3-dithiolan-2-ylidene]-1-imidazolylacetonitrile HA for the manufacturing of luliconazole and pharmaceutically acceptable salts or co-crystals thereof in high yield and purity. The present invention further is directed to this compound R-(-)-(E)-[4-(2,4-dichlorophenyl)-1,3-dithiolan-2-ylidene]-1-imidazolylacetonitrile HA in the treatment of fungal infections.

A switch in enantiomer preference between mitochondrial F1F 0-ATPase chemotypes

Bisaha, Sharon N.,Malley, Mary F.,Pudzianowski, Andrew,Monshizadegan, Hossain,Wang, Paulina,Madsen, Cort S.,Gougoutas, Jack Z.,Stein, Philip D.

, p. 2749 - 2751 (2007/10/03)

The preferred absolute configuration of two series of F1F 0-ATP synthase inhibitors was determined. Although the configuration of the active enantiomer in each series is different, each series presents the same 'triaryl' pharmacophor

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