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1H-Imidazole, 2-[(4-fluorophenyl)thio]-4,5-bis(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81527-20-0

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81527-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81527-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,2 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81527-20:
(7*8)+(6*1)+(5*5)+(4*2)+(3*7)+(2*2)+(1*0)=120
120 % 10 = 0
So 81527-20-0 is a valid CAS Registry Number.

81527-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-fluorophenyl)sulfanyl-4,5-bis(4-methoxyphenyl)-1H-imidazole

1.2 Other means of identification

Product number -
Other names 4,5-Bis(4-methoxyphenyl)-2-(4-fluorphenylthio)-imidazol

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:81527-20-0 SDS

81527-20-0Downstream Products

81527-20-0Relevant academic research and scientific papers

Antiinflammatory imidazole derivatives

-

, (2008/06/13)

Imidazole derivatives of the formula STR1 wherein AR1 and AR2 each independently is phenyl, optionally substituted by halogen atoms, alkyl residues, alkoxy residues; or dialkylamino residues; pyridyl, furyl; or thienyl; R1

Antiinflammatory agents, XVII: 4,5-Bis-(4-methoxyphenyl)-2-(arylthio)azoles with antiinflammatory activity

Klose,Niedballa,Schwarz,Bottcher

, p. 941 - 951 (2007/10/02)

The syntheses of 4,5-bis(4-methoxyphenyl)-2-(arylthio)imidazoles, -thiazoles and -oxazoles are described and their inflammatory activities are compared. Thioethers, sulfoxides, and sulfones of the phenyl, 4-fluorophenyl, and 2-thienyl derivatives were inv

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