179543-88-5

Basic information

• Product Name: 5-Hydrazinyl-2-Methoxypyridine hydrochloride
• Synonyms: 5-Hydrazinyl-2-Methoxypyridine hydrochloride
• CAS NO: 179543-88-5
• Molecular Formula: C₆H₉N₃O*ClH
• Molecular Weight: 175.6161
• Mol File: 179543-88-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 5-Hydrazinyl-2-Methoxypyridine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Hydrazinyl-2-Methoxypyridine hydrochloride(179543-88-5)
• EPA Substance Registry System: 5-Hydrazinyl-2-Methoxypyridine hydrochloride(179543-88-5)

Safety Data

• Hazardous Substances Data: 179543-88-5(Hazardous Substances Data)

Usage

General Description

5-Hydrazinyl-2-Methoxypyridine hydrochloride is a chemical compound with the chemical formula C7H10N4OCl. It is a derivative of pyridine and is commonly used in organic synthesis and pharmaceutical research. 5-Hydrazinyl-2-Methoxypyridine hydrochloride is a hydrazine derivative with a methoxy group attached to the pyridine ring, and the hydrochloride salt form of 5-Hydrazinyl-2-Methoxypyridine is often used for stability and solubility purposes. It is also known to possess antifungal and antiproliferative properties and has shown promising results in cancer research. Additionally, it can be used as a building block in the synthesis of various pharmaceutical compounds and organic materials.

Upstream product

• 6628-77-9 6-methoxy-pyridin-3-ylamine 
• 160664-95-9 5-hydrazinyl-2-methoxy pyridine 

Downstream Products

• 741288-81-3 1-(6-methoxy-pyridin-3-yl)-5-[1-(phenylsulfonyl)pyrrol-2-yl] pyrazole-3-carboxylic acid ethyl ester 
• 858598-00-2 ethyl 5-(3-dimethylaminophenyl)-1-(6-methoxy-3-pyridyl)-1H-pyrazole-3-carboxylate 
• 858598-10-4 ethyl 5-(4-dimethylaminophenyl)-1-(6-methoxy-3-pyridyl)-1H-pyrazole-3-carboxylate 
• 741291-47-4 1-(6-methoxy-3-pyridyl)-5-(3-methylphenyl)pyrazole-3-carboxylic acid ethyl ester 
• 741286-88-4 5-(4-Methoxyphenyl)-1-(6-methoxy-pyridin-3-yl)pyrazole-3-carboxylic acid ethyl ester 
• 160664-95-9 5-hydrazinyl-2-methoxy pyridine 

Relevant articles and documents

Understanding and Interrupting the Fischer Azaindolization Reaction

Experimental and computational studies pertaining to the Fischer azaindolization reaction are reported. These studies explain why pyridylhydrazines are poorly reactive in Fischer indolization reactions, in addition to the origin of hydrazine substituent effects. Additionally, an interrupted variant of Fischer azaindolization methodology is disclosed, which provides a synthetic entryway into fused azaindoline scaffolds.

AMIDOPYRAZOLE DERIVATIVE

A platelet coagulation inhibitor which inhibits neither COX-1 nor COX-2 is provided. The inhibitor is a compound represented by general formula (I): wherein Ar1 and Ar2 independently represent a 5- or 6-membered aromatic heterocyclic group optionally substituted with 1 to 3 substituents, or a phenyl group optionally substituted with 1 to 3 substituents; R1 represents a lower acyl group, carboxyl group, a lower alkoxycarbonyl group, a lower alkoxy group, a lower alkyl group optionally substituted with 1 or 2 substituents, a carbamoyl group optionally substituted with 1 or 2 substituents, an oxamoyl group optionally substituted with 1 or 2 substituents, an amino group optionally substituted with 1 or 2 substituents, a 4- to 7-membered alicyclic heterocyclic group optionally substituted with 1 or 2 substituents, a phenyl group optionally substituted with 1 to 3 substituents, or a 5- or 6-membered aromatic heterocyclic group optionally substituted with 1 to 3 substituents; and R2 represents hydrogen atom, a halogeno group, or the like.