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1-Butanone, 1-(4-fluorophenyl)-4-[1-oxido-4-(2-pyridinyl)-1-piperazinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66065-28-9

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66065-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66065-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,6 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66065-28:
(7*6)+(6*6)+(5*0)+(4*6)+(3*5)+(2*2)+(1*8)=129
129 % 10 = 9
So 66065-28-9 is a valid CAS Registry Number.

66065-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorophenyl)-4-(1-oxido-4-pyridin-2-ylpiperazin-1-ium-1-yl)butan-1-one

1.2 Other means of identification

Product number -
Other names 1-Butanone,1-(4-fluorophenyl)-4-[1-oxido-4-(2-pyridinyl)-1-piperazinyl]

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:66065-28-9 SDS

66065-28-9Upstream product

66065-28-9Downstream Products

66065-28-9Relevant academic research and scientific papers

Fluorescence characteristics of azaperone and of an azaperone mononitrogen oxide

Baeyens,De Moerloose,De Taeye

, p. 1787 - 1789 (1977)

The structure elucidation of the compound isolated after peroxide treatment of azaperone is described. A mononitrogen oxide was formed at the piperazine N1 atom after reaction with excess hydrogen peroxide. The fluorescence characteristics of the derivative were examined and compared with the native fluorescence capacities of the azaperone base; both were identical, depending on the solvent nature. The phenomenon is explained by the fact that the fluorescent properties of the azaperone molecule are principally produced by its ortho-nitrogen substituted pyridine nucleus.

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