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2-Chloro-6-nitropyridine is a chemical compound characterized by the molecular formula C5H3ClN2O2. It presents as a pale yellow crystalline solid and is recognized for its role as an intermediate in the synthesis of various products, including pharmaceuticals and agrochemicals. Additionally, it finds application in the production of dyes and pigments, and is utilized in research and development for the creation of new chemical compounds. Due to its highly flammable nature and potential toxicity, it requires careful handling and adherence to safety protocols to mitigate risks to health and the environment.

94166-64-0

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94166-64-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-6-nitropyridine serves as a crucial intermediate in the synthesis of pharmaceuticals, contributing to the development of new medications and therapeutic agents. Its chemical structure allows for further reactions and modifications that can enhance the properties of resulting compounds, making it a valuable component in drug discovery and production processes.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-6-nitropyridine is utilized as an intermediate in the synthesis of various agrochemicals. Its involvement in the production of pesticides, herbicides, and other agricultural chemicals aids in enhancing crop protection and yield.
Used in Dye and Pigment Production:
2-Chloro-6-nitropyridine is also employed in the manufacturing of dyes and pigments, where its chemical properties contribute to the creation of a wide range of colorants used in different industries, including textiles, plastics, and printing inks.
Used in Research and Development:
2-Chloro-6-nitropyridine plays a significant role in the research and development of new chemical entities. Its reactivity and structural features make it a useful building block for the synthesis of novel compounds with potential applications in various fields, including materials science, chemical engineering, and biotechnology.
Safety Precautions:
Given the potential hazards associated with 2-Chloro-6-nitropyridine, including its flammability and toxicity, it is imperative to follow proper safety measures. This includes using personal protective equipment, handling the compound in well-ventilated areas, and adhering to specific storage and disposal guidelines to prevent accidents and minimize environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 94166-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 94166-64:
(7*9)+(6*4)+(5*1)+(4*6)+(3*6)+(2*6)+(1*4)=150
150 % 10 = 0
So 94166-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3ClN2O2/c6-4-2-1-3-5(7-4)8(9)10/h1-3H

94166-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-chloro-6-nitropyridine

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:94166-64-0 SDS

94166-64-0Relevant academic research and scientific papers

Bismuth nitrate as a source of nitro radical in ipso-nitration of carboxylic acids

Agasti, Soumitra,Maiti, Siddhartha,Maity, Soham,Anniyappan,Talawar,Maiti, Debabrata

, p. 120 - 124 (2019/05/22)

Aromatic nitro compounds are extensively used in synthetic chemistry. We disclose a new approach to obtain nitroarenes regioselectively starting from carboxylic acids under acid-free reaction conditions.

Substituted N-phenyl 2-hydroxy-2-methyl-3,3,3-trifluoropropanamide derivatives which elevate pyruvate dehydrogenase activity

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Page column 61, (2010/02/05)

A compound of formula (I) wherein: n is 1 or 2; R 1 is chloro, fluoro, bromo, methyl or methoxy; R 2 is as defined within; R 3 is as defined within; and R 4 is hydrogen or fluoro; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof is described. The use of compounds of formula (I) in the production of an elevation of PDH activity in a warm-blooded animal such as a human being are also described. Pharmaceutical compositions, methods and processes for preparation of compounds of formula (I) are detailed. STR1

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