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Pyridine, 2-chloro-5-iodo-4-methylis an organic compound belonging to the pyridine family, characterized by the presence of a chloro, iodo, and methyl group at the 2nd, 5th, and 4th positions respectively. It is a versatile chemical intermediate with potential applications in various industries due to its unique structural features.

550347-54-1

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550347-54-1 Usage

Uses

Used in Pharmaceutical Industry:
Pyridine, 2-chloro-5-iodo-4-methylis used as a reactant/reagent for the synthesis of conformationally constrained spirodihydrofuropyridine analogs of epibatidine. These analogs are of significant interest in the pharmaceutical industry due to their potential as therapeutic agents, particularly in the development of novel drugs targeting specific receptors or biological pathways.
Used in Chemical Synthesis:
In the field of chemical synthesis, Pyridine, 2-chloro-5-iodo-4-methylserves as a valuable building block for the creation of more complex molecules. Its unique substitution pattern allows for targeted functionalization and the formation of a diverse range of compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
Pyridine, 2-chloro-5-iodo-4-methylis also utilized in research and development settings, where it can be employed to study the effects of different substituents on the properties and reactivity of pyridine derivatives. This knowledge can be applied to the design and synthesis of new molecules with tailored properties for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 550347-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,0,3,4 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 550347-54:
(8*5)+(7*5)+(6*0)+(5*3)+(4*4)+(3*7)+(2*5)+(1*4)=141
141 % 10 = 1
So 550347-54-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClIN/c1-4-2-6(7)9-3-5(4)8/h2-3H,1H3

550347-54-1SDS

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-5-iodo-4-methylpyridine

1.2 Other means of identification

Product number -
Other names 2-chloro-5-iodo-4-methylpyridine

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:550347-54-1 SDS

550347-54-1Relevant academic research and scientific papers

SPIROCYCLIC ISOXAZOLINES AS ANTIPARASITIC AGENTS

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Page/Page column 62, (2014/03/26)

The invention recites spirocyclic isoxazoline derivatives of Formula (1) stereoisomers thereof, veterinary or pharmaceutical acceptable salts thereof, compositions thereof, processes for making, and their use as a parasiticide in an animal. The variables

Synthesis of conformationally constrained spirodihydrofuropyridine analogues of epibatidine

Abe, Hideki,Arai, Yumiko,Aoyagi, Sakae,Kibayashi, Chihiro

, p. 2971 - 2973 (2007/10/03)

Conformationally constrained spirofuropyridine analogues of epibatidine, syn-2 and anti-2, in which the 7-azabicyclo[2.2.1]heptane system and the 2-chloropyridine ring are held rigidly with the shorter and longer N-N distances, respectively, were synthesized from N-Boc-7-azabicyclo[2.2.1]heptan-2-one. The preliminary binding studies suggested that syn-2 has stronger binding affinity for nAChRs than anti-2.

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