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2-CHLORO-4,6-DIMETHYL-5-NITRO-NICOTINONITRILE is a chemical compound characterized by its molecular formula C8H7ClN4O2. It is a yellow crystalline solid with a molecular weight of 220.62 g/mol. 2-CHLORO-4,6-DIMETHYL-5-NITRO-NICOTINONITRILE is recognized for its potential applications in various fields due to its unique chemical structure and properties.

6220-77-5

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6220-77-5 Usage

Uses

Used in Pharmaceutical Industry:
2-CHLORO-4,6-DIMETHYL-5-NITRO-NICOTINONITRILE is used as an intermediate in the synthesis of various pharmaceutical compounds. Its chemical structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
2-CHLORO-4,6-DIMETHYL-5-NITRO-NICOTINONITRILE is utilized as an intermediate in the production of agrochemicals. Its strong nitro and chloro groups endow it with insecticidal properties, making it a potential candidate for use as a pesticide and insecticide in agricultural applications.
Used in Organic Chemistry:
2-CHLORO-4,6-DIMETHYL-5-NITRO-NICOTINONITRILE serves as a building block for the synthesis of pyrimidine-based compounds and various heterocycles. Its unique structure makes it valuable in the creation of complex organic molecules, expanding the scope of organic synthesis.
It is crucial to handle 2-CHLORO-4,6-DIMETHYL-5-NITRO-NICOTINONITRILE with care due to its potential health and environmental hazards if not properly managed. Safe handling protocols should be strictly followed to mitigate any risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 6220-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6220-77:
(6*6)+(5*2)+(4*2)+(3*0)+(2*7)+(1*7)=75
75 % 10 = 5
So 6220-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClN3O2/c1-4-6(3-10)8(9)11-5(2)7(4)12(13)14/h1-2H3

6220-77-5SDS

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-4,6-dimethyl-5-nitropyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Chloro-4,6-dimethyl-5-nitro-nicotinonitrile

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:6220-77-5 SDS

6220-77-5Relevant academic research and scientific papers

PYRIDYL COMPOUND SUITABLE FOR THE TREATMENT OF METABOLIC DISORDERS

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Page/Page column 57, (2015/01/16)

The description relates to a pyridyl compound of Formula 1 wherein A, B, X, R1, R2, R3, R4, R5, R6, and n are as defined in the specification, in all their isotopic forms, stereoisomeric and tautomeric forms and mixtures thereof in all ratios, their pharmaceutically acceptable salts, N-oxides, pharmaceutically acceptable solvates, isosteres and prodrugs thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia. The description also relates to a process for the manufacture of the pyridyl compound and a pharmaceutical composition containing the pyridyl compound.

Synthesis of some halogen- and nitro-substituted nicotinic acids and their fragmentation under electron impact

Dyadyuchenko,Strelkov,Mikhailichenko,Zaplishny

, p. 308 - 314 (2007/10/03)

Features of electrophilic and nucleophilic substitution under chlorination and nitration reactions conditions have been investigated for 6-hydroxy- and 6-methyl-substituted derivatives of 3-cyano-4-methyl-2(1H)-pyridones. The polychloro- and nitro-substituted 3-cyano-4-methylpyridines obtained were used as synthons in the synthesis of some polyhalo- and nitro-substituted nicotinic acids and their amides. The fragmentation pathways of the synthesized compounds under electron impact have been studied.

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