6311-92-8

Basic information

• Product Name: 3-N-HEXYLPYRIDINE
• Synonyms: 3-HEXYLPYRIDINE;3-N-HEXYLPYRIDINE;3-n-Hexylpyridine, 98+%
• CAS NO: 6311-92-8
• Molecular Formula: C₁₁H₁₇N
• Molecular Weight: 163.26
• Mol File: 6311-92-8.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 242.1 °C at 760 mmHg
• Flash Point: 110.1 °C
• Appearance: /
• Density: 0,903 g/cm3
• Vapor Pressure: 0.0538mmHg at 25°C
• Refractive Index: 1.489
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-N-HEXYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-N-HEXYLPYRIDINE(6311-92-8)
• EPA Substance Registry System: 3-N-HEXYLPYRIDINE(6311-92-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 6311-92-8(Hazardous Substances Data)

Usage

General Description

3-N-Hexylpyridine is a chemical compound with the molecular formula C11H17N. It is a clear, colorless to light yellow liquid with a strong, unpleasant odor. 3-N-Hexylpyridine is commonly used as an intermediate for the synthesis of pharmaceuticals and agrochemicals. It is also used as a flavoring agent in the food industry due to its aromatic properties. In addition, this chemical is employed in the production of corrosion inhibitors, lubricants, and surfactants. However, 3-N-Hexylpyridine is considered to be harmful if swallowed, inhaled, or absorbed through the skin and can cause irritation to the respiratory system and skin. Therefore, proper precautions and safety measures should be taken when handling this chemical.

InChI:InChI=1/C11H17N/c1-2-3-4-5-7-11-8-6-9-12-10-11/h6,8-10H,2-5,7H2,1H3

Upstream product

• 108-99-6 3-Methylpyridine 
• 1120-90-7 3-iodopyridine 
• 72253-33-9 diethyl pyridin-3-yl phosphate 
• 44767-62-6 n-hexylmagnesium chloride 
• 1132-27-0 pyridin-3-yl dimethylsulfamate 
• 51581-40-9 3-pyridyl diethylcarbamate 
• 626-55-1 3-Bromopyridine 
• 111-25-1 1-bromo-hexane 
• 3761-92-0 n-hexylmagnesium bromide 
• 110-89-4 piperidine 
• 111-27-3 hexan-1-ol 
• 7335-01-5 1-hexylpiperidine 

Downstream Products

• 948559-97-5 1-[2-deoxy-3,5-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyl]-5-[2-(5-hexylpyrid-2-yl)ethynyl]uracil 

Relevant articles and documents

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

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Ionic iron (II) composition as well as preparation method and application thereof

The invention discloses an ionic iron (II) composition as well as a preparation method and application thereof. The ionic iron (II) composition contains phosphine ligands and imidazole (quinoline) cations, and the general formula of the ionic iron (II) is [Fe(PR3)X3][(R1NCHnCHnNR1)CH], wherein X is selected from one of chlorine or bromine. The ionic iron (II) composition containing the phosphine ligands and the imidazole (quinoline) cations can efficiently catalyze a phosphoric acid aryl diethyl ester compound and an alkyl group Grignard reagent to perform a crisscross coupling reaction, and particularly can effectively catalyze an unactivated phosphoric acid aryl diethyl ester compound and the alkyl group Grignard reagent to perform the reaction.

Unprecedented Negishi coupling at C-Br in the presence of a stannyl group as a convenient approach to pyridinylstannanes and their application in liquid crystal synthesis

(Chemical Equation Presented) The 2-bromo-5(or 6)-tri-n- butylstannylpyridines, prepared from dibromopyridines and i-PrMgCl at room temperature, undergo Negishi coupling with either alkyl or arylzinc chlorides. The new alkyl- and aryl-substituted pyridylstannanes produced are shown to be suitable for further functionalization by Stille coupling. A group of new liquid crystalline materials with aromatic cores comprised of pyridine and thiophene rings were prepared utilizing these new pyridinylstannanes as key intermediates.