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18344-58-6

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18344-58-6 Usage

General Description

3,5-Dichloro-4-nitropyridine N-oxide is a chemical compound with the molecular formula C5H2Cl2N3O3. It is a yellow to orange solid that is insoluble in water and has a melting point in the range of 135-137 degrees Celsius. 3,5-DICHLORO-4-NITROPYRIDINE N-OXIDE is mainly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used as a building block in the development of other chemical compounds. The chemical has potential applications in the pharmaceutical and agricultural industries due to its unique properties and reactivity. Additionally, it has been studied for its potential use in organic synthesis and as a reagent in various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 18344-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,4 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18344-58:
(7*1)+(6*8)+(5*3)+(4*4)+(3*4)+(2*5)+(1*8)=116
116 % 10 = 6
So 18344-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H2Cl2N2O3/c6-3-1-8(10)2-4(7)5(3)9(11)12/h1-2H

18344-58-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dichloro-4-nitro-1-oxidopyridin-1-ium

1.2 Other means of identification

Product number -
Other names 3,5-Dichloro-4-nitropyridine 1-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:18344-58-6 SDS

18344-58-6Relevant articles and documents

Johnson et al.

, p. 1235 (1967)

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