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Pyridine,4-chloro-2,6-dimethoxy-, also known as 4-Chloro-2,6-dimethoxy-pyridine, is a white to off-white crystalline solid belonging to the pyridine family of chemical compounds. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Pyridine,4-chloro-2,6-dimethoxyhas a strong odor and is considered hazardous, as it can irritate the skin, eyes, and respiratory system upon contact or inhalation. Its derivative compounds have potential applications in the pharmaceutical and agricultural industries, and it has been studied for its potential biological and pharmacological activities, including effects on the central nervous system and potential anticancer properties.

62616-14-2

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62616-14-2 Usage

Uses

Used in Pharmaceutical Industry:
Pyridine,4-chloro-2,6-dimethoxyis used as an intermediate in the synthesis of various pharmaceuticals for its potential biological and pharmacological activities. Its derivative compounds contribute to the development of new drugs in the industry.
Used in Agrochemical Industry:
Pyridine,4-chloro-2,6-dimethoxyserves as an intermediate in the synthesis of agrochemicals, playing a crucial role in the development of pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Chemical Research:
Pyridine,4-chloro-2,6-dimethoxyis utilized in chemical research for studying its potential applications and properties, including its effects on the central nervous system and its potential anticancer properties, contributing to the advancement of scientific knowledge in the field.
Used in Organic Compounds Synthesis:
Pyridine,4-chloro-2,6-dimethoxyis used as an intermediate in the synthesis of various organic compounds, facilitating the creation of new chemical entities for diverse applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 62616-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,1 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62616-14:
(7*6)+(6*2)+(5*6)+(4*1)+(3*6)+(2*1)+(1*4)=112
112 % 10 = 2
So 62616-14-2 is a valid CAS Registry Number.

62616-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2,6-dimethoxypyridine

1.2 Other means of identification

Product number -
Other names 4-chloro-2,6-dimethoxy-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:62616-14-2 SDS

62616-14-2Downstream Products

62616-14-2Relevant academic research and scientific papers

N-HETEROARYL COMPOUNDS WITH CYCLIC BRIDGING UNIT FOR THE TREATMENT OF PARASITIC DISEASES

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Page/Page column 95, (2012/04/17)

This invention relates to certain N-heteroaryl compounds that are generally useful as medicaments, more specifically as medicaments for animals. The medicament can preferably be used for the treatment of helminth infections and the treatment of parasitosis, such as caused by helminth infections. This invention also relates to uses of the compounds to make medicaments and treatments comprising the administration of the compounds to animals in need of the treatments. This invention also relates to the preparation of the N-heteroaryl compounds. Moreover this invention relates to pharmaceutical compositions and kits comprising the compounds.

Novel Annelation Method to Pyridine and Isoquinoline by Photochemical Means

Kaneko, Chikara,Uchiyama, Keiji,Sato, Masayuki,Katagiri, Nobuya

, p. 3658 - 3671 (2007/10/02)

Intramolecular photoaddition reactions of 2-(ω-alkenyl)isoquinolin-1(2H)-ones and 1-(ω-alkenyl)pyridin-2(1H)-ones were examined, and the regioselectivity and dependence of these reactions on the length of methylene chain in the alkenyl group were clarified.By utilizing these reactions, a synthetic route to indolizine and quinolizine derivates was elaborated.By an extension of this approach to the intermolecular reaction, 6-methoxy-3-methyl-1,2-dihydrocyclobutapyridin-4(3H)-one was synthesized from 4,6-dimethoxy-1-methylpyridin-2(1H)-one.Keywords-2+2 photocycloaddition; intramolecular photoaddition; photocycloreversion; annelation; indolizine; quinolizine; cyclobutapyridine; 4,6-dimethoxypyridin-2(1H)-one; 1-(ω-alkenyl)pyridin-2(1H)-one; 2-(ω-alkenyl)isoquinolin-1(2H)-one

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