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

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

Uses

Used in Pharmaceutical Research:
5-Hydrazinyl-2-Methoxypyridine hydrochloride is used as a research compound for its antifungal and antiproliferative properties, making it a valuable tool in the development of new pharmaceuticals targeting fungal infections and cancer.
Used in Organic Synthesis:
As a building block in organic synthesis, 5-Hydrazinyl-2-Methoxypyridine hydrochloride is utilized for the creation of various pharmaceutical compounds and organic materials, contributing to the advancement of chemical and material sciences.
Used in Cancer Research:
5-Hydrazinyl-2-Methoxypyridine hydrochloride is employed as a potential anticancer agent, showing promise in studies for its ability to inhibit the growth and proliferation of cancer cells, warranting further investigation into its therapeutic applications in oncology.
Used in Fungal Infection Treatment:
5-Hydrazinyl-2-Methoxypyridine hydrochloride is used as an antifungal agent, leveraging its properties to combat fungal infections, offering a potential alternative or adjunct to existing antifungal treatments in the medical field.

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.

PYRAZOLE DERIVATIVE

A compound represented by Formula (I): wherein Ar1 represents Formula (II): Ar2 represents a 5- or 6-membered aromatic heterocyclic group which may be substituted; and X represents Formula (III): a salt thereof, or a solvate of the compound or the salt. A potent platelet aggregation suppressant which does not inhibit COX-1 and COX-2 is provided.

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.

PYRAZOLE DERIVATIVE

Not available