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2-Chloro-3-iodo-4-methylpyridine is a chemical compound with the molecular formula C6H5ClIN. It is a derivative of pyridine, featuring a chlorine atom at the 2 position, an iodine atom at the 3 position, and a methyl group at the 4 position. 2-Chloro-3-iodo-4-methylpyridine is known for its high reactivity and is utilized in various chemical processes, particularly in the synthesis of pharmaceuticals and agrochemicals.

926922-28-3

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926922-28-3 Usage

Uses

Used in Organic Synthesis:
2-Chloro-3-iodo-4-methylpyridine is used as a reagent in organic synthesis for its ability to participate in a wide range of chemical reactions. Its unique structure allows it to be a versatile building block in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloro-3-iodo-4-methylpyridine is used as an intermediate in the production of various pharmaceuticals. Its presence in the synthesis process contributes to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2-Chloro-3-iodo-4-methylpyridine is employed as an intermediate for the synthesis of pesticides and other agricultural chemicals. Its role in these processes helps in the development of effective products for crop protection and enhancement of agricultural yields.
Used in Production of Fine Chemicals:
2-Chloro-3-iodo-4-methylpyridine also finds application in the production of fine chemicals, where its reactivity and structural features are leveraged to create specialty chemicals used in various industries, including fragrances, dyes, and other high-value chemical products.
Safety Considerations:
Due to its high reactivity, 2-Chloro-3-iodo-4-methylpyridine should be handled with care by trained professionals to avoid potential hazards. Proper safety measures and protocols must be followed during its use in laboratories and industrial settings to ensure the safety of personnel and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 926922-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,9,2 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 926922-28:
(8*9)+(7*2)+(6*6)+(5*9)+(4*2)+(3*2)+(2*2)+(1*8)=193
193 % 10 = 3
So 926922-28-3 is a valid CAS Registry Number.

926922-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-3-iodo-4-methylpyridine

1.2 Other means of identification

Product number -
Other names -

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:926922-28-3 SDS

926922-28-3Relevant academic research and scientific papers

HERBICIDAL PYRIDAZINONE DERIVATIVES

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Page/Page column, (2014/09/29)

The present invention provides a compound of Formula (I) or an agronomically acceptable salt thereof, wherein: R2 is selected from the group consisting of (A1), (A2) and (A3) wherein X1 is N or CR7X2 is N or CR8X3 is N or CR9X4 is N or CR6R1, R3, R4, R5 R6, R7, R8 and R9 are as defined herein. The invention further relates to herbicidal compositions which comprise a compound of Formula (I), and to their use for controlling weeds, in particular in crops of useful plants.

Indolin-2-one p38α inhibitors III: Bioisosteric amide replacement

Eastwood, Paul,González, Jacob,Gómez, Elena,Caturla, Francisco,Aguilar, Nuria,Mir, Marta,Aiguadé, Josep,Matassa, Victor,Balagué, Cristina,Orellana, Adelina,Domínguez, María

scheme or table, p. 6253 - 6257 (2011/11/29)

Crystallographic structural information was used in the design and synthesis of a number of bioisosteric derivatives to replace the amide moiety in a lead series of p38a inhibitors which showed general hydrolytic instability in human liver preparations. Triazole derivative 13 was found to have moderate bioavailability in the rat and demonstrated potent in-vivo activity in an acute model of inflammation.

New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors

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Page/Page column 37, (2009/12/04)

This invention is directed to new inhibitors of the p38 mitogen-activated protein kinase having the general formula (I) to processes for their preparation; to pharmaceutical compositions comprising them; and to their use in therapy.

UNSATURATED HETEROCYCLIC DERIVATIVES

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Page/Page column 40, (2008/06/13)

This invention relates to compounds of the general formula: in which the variable groups are as defined herein, and to their preparation and use.

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