145934-89-0

Basic information

• Product Name: Pyridine, 2-chloro-5-hydrazino- (9CI)
• Synonyms: Pyridine, 2-chloro-5-hydrazino- (9CI);2-Chloro-5-hydrazinopyridine;(6-Chloro-pyridin-3-yl)-hydrazine;2-chloro-5-hydrazinylpyridine;Pyridine,2-chloro-5-hydrazinyl-;2-chloro-5-hydrazino-pyridine(9CI)
• CAS NO: 145934-89-0
• Molecular Formula: C5H6ClN3
• Molecular Weight: 143.57424
• Product Categories: PYRIDINE
• Mol File: 145934-89-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 127 °C
• Boiling Point: 307.2±27.0 °C(Predicted)
• Appearance: /
• Density: 1.418±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
• PKA: 4.10±0.24(Predicted)
• CAS DataBase Reference: Pyridine, 2-chloro-5-hydrazino- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 2-chloro-5-hydrazino- (9CI)(145934-89-0)
• EPA Substance Registry System: Pyridine, 2-chloro-5-hydrazino- (9CI)(145934-89-0)

Safety Data

• Hazardous Substances Data: 145934-89-0(Hazardous Substances Data)

Usage

General Description

Pyridine, 2-chloro-5-hydrazino- (9CI) is a specialized chemical typically used in laboratory settings for a variety of applications. As a derivative of pyridine, it demonstrates a similar basic structure with an added hydrazino group at the 5-position and a chlorine atom at the 2-position. This configuration, combined with the inherent reactivity of the hydrazino group, makes this chemical a useful component in a number of reactions and synthesis procedures. As with any laboratory-grade chemical, it requires proper safety measures and precautions when handling due to its potential hazards, such as health risks and reactivity. Specific properties such as melting point, boiling point, solubility, and others may vary depending on purity and other factors.

Upstream product

• 478361-25-0 2-chloro-5-pyridylsydnone 
• 5350-93-6 6-Chloro-pyridin-3-ylamine 
• 478361-24-9 N-nitroso-N-(2-chloro-5-pyridyl)glycine 
• 31301-51-6 2-chloro-5-fluoropyridine 

Relevant articles and documents

Extending the scope of the aza-Fischer synthesis of 4- and 6-azaindoles

Fischer indole cyclization has recently been described as an efficient approach to the synthesis of azaindoles bearing electron-donating groups. We now show that this cascade reaction can be very efficient for the formation of a wider range of 4- and 6-azaindoles by using microwave irradiation. Fischer indole cyclization starting from aminopyridines is a very efficient cascade sequence leading to 4- and 6-azaindoles. The scope of the substituents on the pyridine ring was extended to include halogens and to weakly electron-donating substituents by using microwave irradiation. Copyright

INDOLIN PHENYLSULFONAMIDE DERIVATIVES

The invention relates to novel substituted indolin phenylsulfonamide derivatives, to a method for the production thereof and to the use thereof in medicaments, especially as potent PPAR-delta activating compounds for the prophylaxis and/or treatment of cardiovascular diseases, especially dyslipidaemia and coronary heart diseases.

ACTIVE COMPOUNDS

Therapeutically active compounds of the formula: wherein the variables are defined in the specification are provided