119285-06-2

Basic information

• Product Name: 3-Pyridinamine,6-(1-piperazinyl)-(9CI)
• Synonyms: 3-Pyridinamine,6-(1-piperazinyl)-(9CI);6-PIPERAZIN-1-YLPYRIDIN-3-AMINE;6-(1-piperazinyl)-3-Pyridinamine;6-(1-piperazinyl)-3-pyridinylamine
• CAS NO: 119285-06-2
• Molecular Formula: C₉H₁₄N₄
• Molecular Weight: 178.23
• Product Categories: PIPERIDINE
• Mol File: 119285-06-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Pyridinamine,6-(1-piperazinyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinamine,6-(1-piperazinyl)-(9CI)(119285-06-2)
• EPA Substance Registry System: 3-Pyridinamine,6-(1-piperazinyl)-(9CI)(119285-06-2)

Safety Data

• Hazardous Substances Data: 119285-06-2(Hazardous Substances Data)

Upstream product

• 82205-58-1 1-(5-nitro-2-pyridinyl)piperazine 
• 4548-45-2 2-chloro-5-nitropyridine 
• 4487-59-6 2-bromo-5-nitropyridine 
• 193902-78-2 tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 

Downstream Products

• 849145-80-8 2-(4-carbobenzyloxypiperazin-1-yl)-5-(carbobenzyloxyamino)pyridine 
• 849145-81-9 (R)-(3-(6-(4-carbobenzyloxypiperazin-1-yl)-pyridin-3-yl)-2-oxo-5-oxazolidinyl)methanol 
• 849145-83-1 (R)-(3-(6-(4-carbobenzyloxypiperazin-1-yl)-pyridin-3-yl)-2-oxo-5-oxazolidinyl)methyl azide 
• 849145-82-0 4-[5-((R)-5-Methanesulfonyloxymethyl-2-oxo-oxazolidin-3-yl)-pyridin-2-yl]-piperazine-1-carboxylic acid benzyl ester 
• 849145-84-2 4-{5-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-pyridin-2-yl}-piperazine-1-carboxylic acid benzyl ester 
• 849145-88-6 N-(3-{6-[4-(4-nitro-benzenesulfonyl)-piperazin-1-yl]-pyridin-3-yl}-2-oxo-oxazolidin-5-ylmethyl)-acetamide 
• 849145-89-7 N-(3-{6-[4-(4-amino-benzenesulfonyl)-piperazin-1-yl]-pyridin-3-yl}-2-oxo-oxazolidin-5-ylmethyl)-acetamide 

Relevant articles and documents

Synthesis and solid state study of pyridine- and pyrimidine-based fragment libraries

A library of pyridines and pyrimidines has been synthesised in excellent yields employing microwave and flow chemistry methodologies. Work-up bottlenecks have been facilitated substantially by the use of supported reagents and many of the final compounds have been studied in the solid state by single crystal X-ray diffraction.

Syntheses and antibacterial activity of a series of 3-(pyridine-3-yl)-2- oxazolidinone

The syntheses of substituted piperazinyl pyridyl oxazolidinones 8-16 are described. Their in vitro activities against Gram-positive organisms such as Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus and enterococcus were evaluated by minim