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13194-60-0

13194-60-0

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13194-60-0 Usage

General Description

3-Chloro-4-nitropyridine is a chemical compound with the molecular formula C5H3ClN2O2. It is a yellow crystalline solid that is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. This chemical is known for its potent nitro and pyridine functionalities, making it a valuable building block for researchers and manufacturers. 3-Chloro-4-nitropyridine is also utilized in the production of dyes, pigments, and other specialty chemicals, making it an important ingredient in various industrial applications. However, it is important to handle this compound with caution, as it may pose health and environmental risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 13194-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,9 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13194-60:
(7*1)+(6*3)+(5*1)+(4*9)+(3*4)+(2*6)+(1*0)=90
90 % 10 = 0
So 13194-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3ClN2O2/c6-4-3-7-2-1-5(4)8(9)10/h1-3H

13194-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4-nitropyridine

1.2 Other means of identification

Product number -
Other names 3-chloro-4-nitro-pyridine

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:13194-60-0 SDS

13194-60-0Relevant articles and documents

A Journey through Hemetsberger–Knittel, Leimgruber–Batcho and Bartoli Reactions: Access to Several Hydroxy 5- and 6-Azaindoles

Radix, Sylvie,Hallé, Fran?ois,Mahiout, Zahia,Teissonnière, Amélie,Bouchez, Grégoire,Auberger, Ludovic,Barret, Roland,Lomberget, Thierry

, (2022/02/22)

The preparation of various 5- and 6-azaindoles, heterocyclic structures that are frequently part of molecules in clinical development, and their monohydroxy analogues were described. Different strategies, relying on the de novo pyrrole ring formation, were investigated and, thanks to Hemetsberger–Knittel, Bartoli and Leimgruber–Batcho approaches, 4- and 7-monohydroxy 5- and 6-azaindoles were obtained. The crucial introduction of the oxygen atom was carried out from halogen derivatives, using nucleophilic substitution reactions under basic conditions with or without a copper catalyst. Some preliminary oxidation reactions have shown that it was yet not possible to synthesize the azaquinone indole structure from monohydroxy azaindole, using molecular oxygen in the presence of salcomine as a catalyst.

[2-[(Nitropyridinyl)amino]phenyl]arymethanones

-

, (2008/06/13)

[2-[(Nitropyridinyl)amino]phenyl]arylmethanones as chemical intermediates and/or having antidepressant activity having the formula: STR1 wherein: B is carbonyl, thioxomethyl, ketal or thioketal, R is hydrogen or -alk1 -Q, Q is hydrogen, --NR1 R2 or halogen are disclosed in a process for preparing pyrido[1,4]benzodiazepines.

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