14159-55-8

Basic information

• Product Name: 2-(1-cyclohexen-1-yl)pyridine
• Synonyms: 2-(1-cyclohexen-1-yl)pyridine;2-(1-Cyclohexenyl)pyridine;Einecs 238-002-0
• CAS NO: 14159-55-8
• Molecular Formula: C₁₁H₁₃N
• Molecular Weight: 159.22762
• EINECS: 238-002-0
• Mol File: 14159-55-8.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 268.2°Cat760mmHg
• Flash Point: 113.5°C
• Appearance: /
• Density: 1.026g/cm³
• Vapor Pressure: 0.0129mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: 2-(1-cyclohexen-1-yl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-cyclohexen-1-yl)pyridine(14159-55-8)
• EPA Substance Registry System: 2-(1-cyclohexen-1-yl)pyridine(14159-55-8)

Safety Data

• Hazardous Substances Data: 14159-55-8(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Odor

Strong and pungent

Uses

Production of pharmaceuticals, agrochemicals, fragrance ingredient in perfumes, and flavor ingredient in food products

Chemical stability

High

Solubility

Soluble in organic solvents such as ethanol and acetone

Safety precautions

May be harmful if inhaled or swallowed, can cause skin and eye irritation upon contact

InChI:InChI=1/C11H13N/c1-2-6-10(7-3-1)11-8-4-5-9-12-11/h4-6,8-9H,1-3,7H2

Upstream product

• 41727-18-8 1-(pyridin-2-yl)cyclohexanol 
• 108-94-1 cyclohexanone 
• 109-04-6 2-bromo-pyridine 
• 89490-05-1 cyclohex-1-enylboronic acid 
• 109-09-1 2-chloropyridine 
• 141091-37-4 2-(cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 2044-08-8 1-bromocyclohex-1-ene 
• 1402132-80-2 C₁₁H₁₅N₃ 
• 61835-95-8 cyclohexanone 2,4,6-triisopropylbenzenesulphonylhydrazone 
• 110-86-1 pyridine 

Downstream Products

• 952599-10-9 1-[4-(2-pyridin-2-ylcyclohex-1-en-1-yl)phenyl]ethanone 
• 1161621-87-9 1-[2-(2-pyridyl)-1-cyclohexenyl]pentan-3-one 
• 1161621-99-3 2-[(E)-2-(1-dodecenyl)-1-cyclohexenyl]pyridine 
• 1161621-90-4 N,N-dimethyl-3-[2-(2-pyridyl)-1-cyclohexenyl]propionamide 
• 1161621-73-3 2-ethylhexyl 3-[2-(2-pyridyl)-1-cyclohexenyl]propionate 
• 1161621-96-0 (E)-2-(2-styrylcyclohex-1-en-1-yl)pyridine 
• 1393679-65-6 C₂₆H₂₅F₃N₂O₂S 
• 1393679-66-7 C₂₅H₂₅FN₂O₂S 
• 1393679-67-8 C₂₅H₂₅FN₂O₂S 
• 1393679-69-0 C₂₆H₂₈N₂O₂S 
• 1393679-70-3 C₂₆H₂₈N₂O₂S 
• 1393679-71-4 C₂₃H₂₄N₂O₂S₂ 
• 1393679-73-6 C₁₈H₁₇ClN₂O₃ 
• 1393679-60-1 C₂₅H₂₆N₂O₂S 

Relevant articles and documents

Transition metal complex, polymer, mixture, composition and organic electronic device

The invention discloses a transition metal complex. The complex is represented by general formula (1) shown in the specification, G in the specification is selected from cycloalkane or a cage group, and the cage group is coordinated with a metal center in a monovalent anion form to obtain a more stable complex structure. The transition metal complex provided by the invention is used in an OLED, especially as a luminescent layer doping material, not only can provide higher luminous efficiency and longer device life, but also can improve the brightness and current efficiency of the device, and meanwhile, reduces the starting voltage to prolong the service life of the device.

Borane-Catalyzed Chemoselective and Enantioselective Reduction of 2-Vinyl-Substituted Pyridines

Herein, we report that highly chemoselective and enantioselective reduction of 2-vinyl-substituted pyridines has been achieved for the first time. The reaction, which uses chiral spiro-bicyclic bisboranes as catalysts and HBpin and an acidic amide as reducing reagents, proceeds through a cascade process involving 1,4-hydroboration followed by transfer hydrogenation of a dihydropyridine intermediate. The retained double bond in the reduction products permits their conversion to natural products and other useful heterocyclic compounds by simple transformations.

Green phosphorescent compound and organic electroluminescent device using same

The invention discloses a green phosphorescent compound and an organic electroluminescent device using the same. The organic electroluminescent device includes an anode, a hole injection layer, a holetransport layer, a light emitting layer, an electron transport layer, an electron injection layer and a cathode which are sequentially deposited from each other. The organic electroluminescent devicecan use a phosphorescent compound represented by a following formula (1) as a dopant for the light emitting layer, wherein R1, R2, R3, R4, R5, R6, R7, R8 and R9 are each independently substituted orunsubstituted C1-C6 alkyl, C1-C6 alkoxyl, or halogens. The green phosphorescent material has the advantages of high efficiency, high color purity and narrow spectrum effect.