173435-34-2

Basic information

• Product Name: 3-Pyridinamine, 2-chloro-4-methoxy-
• Synonyms: 3-Pyridinamine, 2-chloro-4-methoxy-;3-Amino-2-chloro-4-methoxypyridine;2-Chloro-4-Methoxy-pyridin-3-ylaMine;2-Chloro-4-Methoxy-3-pyridinaMine
• CAS NO: 173435-34-2
• Molecular Formula: C₆H₇ClN₂O
• Molecular Weight: 158.59
• Mol File: 173435-34-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 288℃
• Flash Point: 128℃
• Appearance: /
• Density: 1.311
• Vapor Pressure: 0.00232mmHg at 25°C
• Refractive Index: 1.578
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Pyridinamine, 2-chloro-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinamine, 2-chloro-4-methoxy-(173435-34-2)
• EPA Substance Registry System: 3-Pyridinamine, 2-chloro-4-methoxy-(173435-34-2)

Safety Data

• Hazardous Substances Data: 173435-34-2(Hazardous Substances Data)

Usage

General Description

3-Pyridinamine, 2-chloro-4-methoxy- is a chemical compound with the molecular formula C6H6ClNO. It is a derivative of pyridine and contains a chlorine atom and a methoxy group attached to the second and fourth carbon atoms of the pyridine ring, respectively. 3-Pyridinamine, 2-chloro-4-methoxy- is commonly used in the synthesis of pharmaceuticals and agrochemicals. It has various applications in the fields of organic chemistry, medicinal chemistry, and drug development. It is important to handle this chemical with care and follow proper safety protocols when working with it in a laboratory setting.

InChI:InChI=1/C6H7ClN2O/c1-10-4-2-3-9-6(7)5(4)8/h2-3H,8H2,1H3

Upstream product

• 33631-09-3 4-methoxypyridin-3-amine 

Downstream Products

• 958000-12-9 1-(2-Chloro-4-methoxy-pyridin-3-yl)-3-[4-hydroxy-4-(3-trifluoromethylphenyl)-piperidine-1-carbonyl]-thiourea 

Relevant articles and documents

HETEROCYCLIC COMPOUND

Provided is a compound having a superior PKC inhibitory action, and useful as a prophylactic or therapeutic agent for immune diseases, inflammatory diseases and the like, or a salt thereof. A compound represented by the formula (I): wherein each symbol is

N-aryl[1,2,4]triazolo[1,5-a]pyrazine-2-sulfonamide herbicides

Substituted N-aryl[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide compounds, such as 5-bromo-N-(2,6-dichlorophenyl)-8-methoxy[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide, were prepared by condensation of a substituted 2-chlorosulfonyl[1,2,4]triazolo[1,5-a]pyrazine compound, such as 5-bromo-2-chlorosulfonyl-8-methoxy[1,2,4]triazolo[1,5-a]pyrazine with a substituted arylamine compound, such as 2,6-dichloroaniline, and found to possess herbicidal utility.

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