128802-98-2

Basic information

• Product Name: CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE
• Synonyms: CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE;CHEMBRDG-BB 5522246;TIMTEC-BB SBB010836;N-(4-Pyridinylmethyl)cyclohexanamine;N-(pyridin-4-ylmethyl)cyclohexanamine(SALTDATA: FREE);N-cyclohexyl-4-Pyridinemethanamine
• CAS NO: 128802-98-2
• Molecular Formula: C12H18N2
• Molecular Weight: 190.28
• Mol File: 128802-98-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 314.9°Cat760mmHg
• Flash Point: 144.2°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.000453mmHg at 25°C
• Storage Temp.: 2-8°C
• CAS DataBase Reference: CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE(128802-98-2)
• EPA Substance Registry System: CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE(128802-98-2)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 22
• HazardClass: IRRITANT
• Hazardous Substances Data: 128802-98-2(Hazardous Substances Data)

Usage

General Description

CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE is a chemical compound that belongs to the class of cyclohexylamines and pyridines. It is a hybrid molecule that combines the structural features of both cyclohexylamine and pyridine, making it potentially useful in a variety of chemical reactions and synthetic processes. CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE may have applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and potential reactivity. Further research and development into the properties and applications of CYCLOHEXYL-PYRIDIN-4-YLMETHYL-AMINE may uncover new potential uses and benefits in various industries.

InChI:InChI=1/C12H18N2/c1-2-4-12(5-3-1)14-10-11-6-8-13-9-7-11/h6-9,12,14H,1-5,10H2/p+1

Upstream product

• 872-85-5 pyridine-4-carbaldehyde 
• 108-91-8 cyclohexylamine 

Relevant articles and documents

Anchored Palladium Complex-Generated Clusters on Zirconia: Efficiency in Reductive N-Alkylation of Amines with Carbonyl Compounds under Hydrogen Atmosphere

Carbon-nitrogen bond formation is an important method on both laboratory and industrial scales because it realizes the production of valuable pharmaceuticals, agrochemicals, and fine chemicals. Direct reductive N-alkylation of amines with carbonyl compounds via intermediary imine compounds, especially under catalytic hydrogenation conditions, is one of the most convenient, economical, and environmentally friendly methods for this process. Here we report a novel palladium species on zirconia having specific activity towards hydrogenation of imines but other carbonyl groups remaining intact. The present catalytic property offers a practical synthetic method of functionalized secondary amines by reductive N-alkylation under mild conditions with high atom-efficiency. Mechanistic studies revealed that the catalytically active species is the palladium cluster, which is generated in situ from molecular palladium complexes on the support by exposure to atmospheric hydrogen. These fundamental findings are expected to progress in developing novel cluster catalysts for chemical processes directed towards a sustainable society.