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2,3,4,5,6-Pentachloro-1-pyridiniumolate is a chemical compound with the molecular formula C5HCl5NO. It is a pyridinium salt derivative known for its strong oxidizing properties and high reactivity towards various organic compounds. 2,3,4,5,6-PENTACHLORO-1-PYRIDINIUMOLATE is commonly used in organic synthesis and as a reactant in chemical reactions, making it a valuable asset in pharmaceutical and agricultural applications. However, it is also a highly toxic and potentially hazardous chemical, necessitating careful handling and disposal measures.

17573-93-2

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17573-93-2 Usage

Uses

Used in Organic Synthesis:
2,3,4,5,6-Pentachloro-1-pyridiniumolate is used as a reactant in organic synthesis for its strong oxidizing properties and high reactivity with various organic compounds. It aids in the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 2,3,4,5,6-Pentachloro-1-pyridiniumolate is used as a catalyst in organic reactions. Its reactivity enables the development of new drug molecules and the improvement of existing ones, contributing to the advancement of medicinal chemistry.
Used in Agricultural Applications:
2,3,4,5,6-Pentachloro-1-pyridiniumolate is also utilized in the agricultural sector, where it serves as a reactant in the synthesis of agrochemicals. Its strong oxidizing properties and reactivity contribute to the development of effective pesticides and other agricultural chemicals.
Safety and Handling:
Due to its highly toxic nature, 2,3,4,5,6-Pentachloro-1-pyridiniumolate requires careful handling and disposal measures. It is essential to follow proper safety protocols, including the use of personal protective equipment, to minimize exposure and potential health risks. Additionally, proper disposal methods should be employed to prevent environmental contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 17573-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17573-93:
(7*1)+(6*7)+(5*5)+(4*7)+(3*3)+(2*9)+(1*3)=132
132 % 10 = 2
So 17573-93-2 is a valid CAS Registry Number.
InChI:InChI=1/C5Cl5NO/c6-1-2(7)4(9)11(12)5(10)3(1)8

17573-93-2SDS

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 2,3,4,5,6-pentachloro-1-oxidopyridin-1-ium

1.2 Other means of identification

Product number -
Other names pentachloropyridine N-oxide

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:17573-93-2 SDS

17573-93-2Relevant academic research and scientific papers

A novel reagent combination for the oxidation of highly electron deficient pyridines to N-oxides: trifluoromethanesulfonic anhydride/sodium percarbonate

Zhu, Xizhen,Kreutter, Kevin D.,Hu, Huaping,Player, Mark R.,Gaul, Micheal D.

, p. 832 - 834 (2008/04/13)

A novel reagent combination, Tf2O/Na2CO3·1.5H2O2, has been developed for the oxidation of highly electron deficient pyridines to their corresponding N-oxides. The N-oxidation reaction, utilizing the in situ generated peracid, proceeds under mild conditions that allow for a number of functional groups and substitution patterns on the pyridine ring.

Fluorinated pyridine N-oxide thrombin modulators and process for N-oxidation of nitrogen containing heteroaryls

-

Page/Page column 9; 11, (2008/06/13)

The present invention describes compounds of Formula I or a pharmaceutically acceptable salt thereof, for the prophylaxis, or treatment of diseases and conditions related to thrombin activity in a mammal. The present invention also relates to a novel method of N-oxidation of nitrogen containing heteroaryls.

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