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5-Chloro-2-ethoxypyridine is a chemical compound with the molecular formula C7H8ClNO. It is a pale yellow to light brown liquid with a sweet, fruity odor.
Used in Pharmaceutical Industry:
5-Chloro-2-ethoxypyridine is used as an intermediate for the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
This chemical compound serves as an intermediate in the production of agrochemicals, playing a role in the development of agricultural products.
Used in Organic Synthesis:
5-Chloro-2-ethoxypyridine is used as a building block in organic synthesis, facilitating the creation of a range of different chemical compounds.
Used in Medicinal Chemistry:
It is utilized in medicinal chemistry for the synthesis of pyridine derivatives and heterocyclic compounds, which are important in the development of new drugs.
Used in Materials Science:
5-Chloro-2-ethoxypyridine also has potential applications in materials science, where it may contribute to the development of novel materials with specific properties.
Safety Note:
It is important to handle 5-chloro-2-ethoxypyridine with care, as it may be harmful if ingested, inhaled, or in contact with the skin or eyes. Proper safety precautions should be followed to prevent any potential hazards to human health and the environment.

22109-30-4

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22109-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22109-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,0 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22109-30:
(7*2)+(6*2)+(5*1)+(4*0)+(3*9)+(2*3)+(1*0)=64
64 % 10 = 4
So 22109-30-4 is a valid CAS Registry Number.

22109-30-4SDS

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-ethoxy-5-chloropyridine

1.2 Other means of identification

Product number -
Other names 5-Chloro-2-ethoxy-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:22109-30-4 SDS

22109-30-4Downstream Products

22109-30-4Relevant academic research and scientific papers

Diazotization of Aminopyridines in the Presence of Camphorsulfonic Acid. Synthesis and Some Properties of Pyridinyl Camphorsulfonates

Erin, K. D.,Filimonov, V. D.,Krasnokutskaya, E. A.,Sanzhiev, A. N.

, p. 922 - 929 (2021/07/22)

Abstract: Diazotization of 2-, 3-, and 4-aminopyridines in the presence of both racemic camphor-10-sulfonic acid and its pure enantiomers led to the formation of the corresponding pyridyl camphorsulfonates in moderate yields. Pyridyl camphorsulonates were

Antimycobacterial cycloartane derivatives from the roots of Trichilia welwistchii C. DC (Meliaceae)

Tsamo, Armelle Tontsa,Fodja Saah, Edwige P.,Langat, Moses K.,Mkounga, Pierre,Kamdem Waffo, Alain Fran?ois,Nkengfack, Augustin Ephrem

, p. 475 - 480 (2021/08/16)

Chemical investigation of the roots of Trichilia welwitschii yielded a cycloartane type terpenoid 28,29-bis-norcycloart-24-en-3β,4α,6α-triol (1), isolated as pure compound for the first time, three coumarins and three sterols. New cycloartane derivatives (1a) and (1b+1c) were obtained by hemi-synthetic reaction of compound 1. The structures of 1a-c were established by spectroscopic methods including 1D and 2D-NMR analysis, HR-EIMS, chemical transformations and by comparison of these data with those of related compounds. Evaluated for their antimycobacterial potential, compound 1 and 1b+1c were determined to show significant activities against Mycobacterium tuberculosis MIC values of 6.25 μg mL-1 while compound 1a displayed weak activity showing MIC > 100 μg mL-1. Compounds 2-4 displayed moderate activity with MIC values range from 12.5 to 50 μg mL-1.

ANTIDIABETIC BICYCLIC COMPOUNDS

-

Page/Page column 196, (2016/04/04)

Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-coupled receptor 40. The compounds of the present invention may be useful in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.

Rhodium-catalysed nucleophilic ring opening reaction of 1- and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines

Kelebekli, Latif

, p. 304 - 308 (2013/07/27)

2-Ethoxy-3- and 5-chloropyridines were obtained from 2,3- and 2,5-dichloropyridine. Reaction of 2,3- and 2,5-dichloropyridines with tBuLi in the presence of furan gave 1- and 3-ethoxy-5,8-epoxy-5,8-dihydroisoquinolines. The rhodium-catalysed ring-opening

Compounds with medicinal effects due to interaction with the glucocorticoid receptor

-

Page/Page column 16-17, (2010/11/27)

The invention provides for compounds having the structure according to the formula I

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