23569-17-7

Basic information

• Product Name: 4-TERT-BUTYLPYRIDINE 1-OXIDE
• Synonyms: 4-TERT-BUTYLPYRIDINE 1-OXIDE
• CAS NO: 23569-17-7
• Molecular Formula: C₉H₁₃NO
• Molecular Weight: 151.21
• Mol File: 23569-17-7.mol
• Article Data: 36

Chemical Properties

• Melting Point: 103.9-104.3 °C
• Boiling Point: 286.6 °C at 760 mmHg
• Flash Point: 127.1 °C
• Appearance: /
• Density: 0.94 g/cm³
• Vapor Pressure: 0.0045mmHg at 25°C
• Refractive Index: 1.491
• PKA: 1.46±0.10(Predicted)
• CAS DataBase Reference: 4-TERT-BUTYLPYRIDINE 1-OXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-TERT-BUTYLPYRIDINE 1-OXIDE(23569-17-7)
• EPA Substance Registry System: 4-TERT-BUTYLPYRIDINE 1-OXIDE(23569-17-7)

Safety Data

• Hazardous Substances Data: 23569-17-7(Hazardous Substances Data)

Usage

General Description

4-tert-butylpyridine 1-oxide is a chemical compound with the molecular formula C11H15NO. It is a derivative of pyridine with a tert-butyl group and an oxygen atom attached to the nitrogen atom. 4-TERT-BUTYLPYRIDINE 1-OXIDE is used as a reagent in organic synthesis and as a stabilizer in some polymer materials. It is also known to possess antioxidant properties and is used in the production of rubber and plastic products to improve their resistance to oxidation and degradation. Additionally, it has potential applications in pharmaceuticals and agrochemicals due to its unique chemical properties.

InChI:InChI=1/C9H13NO/c1-9(2,3)8-4-6-10(11)7-5-8/h4-7H,1-3H3

Upstream product

• 3978-81-2 4-tert-butylpyridine 

Downstream Products

• 42205-73-2 4-tert-butyl-2-cyanopyridine 
• 1277098-69-7 C₂₄H₂₄N₂O 
• 1361941-59-4 2-(1H-pyrazol-1-yl)-4-tert-butylpyridine 
• 41225-63-2 1-(4-tert-butylpyridin-2-yl)ethanone 
• 3978-81-2 4-tert-butylpyridine 
• 55930-28-4 1-Benzyloxy-4-tert-butyl-pyridinium; bromide 
• 29939-31-9 2,4-di-tert-butylpyridine 
• 53911-36-7 4-(tert-butyl)-2-phenylpyridine 
• 81167-60-4 2-chloro-4-(1,1-dimethylethyl)pyridine 
• 1350449-25-0 4-tert-butylpyridine-2,6-bis[2-(4,6-di-tert-butylphenol)] 

Relevant articles and documents

Synthesis and structural characterization of tris(2-pyridonyl)methyl complexes of zinc and thallium: A new class of metallacarbatranes and a monovalent thallium alkyl compound

Tris(2-pyridonyl)methanes may be synthesized via the reactions of the respective 2-pyridone with CHX3 (X = Cl, Br) and K2CO 3 in the presence of [Bun4N]Br, followed by acid-catalyzed isomerization wit

Substituted 2,2′-bipyridines by nickel catalysis: 4,4′-Di- tert -butyl-2,2′-bipyridine

A simple, ligand-free synthesis of the important bipyridyl ligand 4,4′-di-tert-butyl-2,2′-bipyridine is presented. 5,5′-Bis(trifluoromethyl)-2,2′-bipyridine is also synthesized by the same protocol. The syntheses efficiently couple the parent 2-chloropyridines by a nickel-catalyzed dimerization with manganese powder as the terminal reductant. Georg Thieme Verlag Stuttgart New York.

MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR

This disclosure provides modulators of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), pharmaceutical compositions containing at least one such modulator, methods of treatment of cystic fibrosis using such modulators and pharmaceutical compositions, and processes for making such modulators.

Electrochemical Deoxygenation of N-Heteroaromatic N -Oxides

An electrochemical method for the deoxygenation of N-heteroaromatic N -oxide to give the corresponding N-heteroaromatics has been developed. Several classes of N-heterocycles such as pyridine, quinoline, isoquinoline, and phenanthridine are tolerated. The electrochemical reactions proceed efficiently in aqueous solution without the need for transition-metal catalysts and waste-generating reducing reagents.