4383-25-9

Basic information

• Product Name: N-BENZYLCYCLOHEXYLAMINE
• Synonyms: Benzyl(cyclohexyl)amine;Benzylcyclohexylamine;Cyclohexylbenzylamine;N-Cyclohexylbenzylamine;N-(phenylmethyl)cyclohexanamine
• CAS NO: 4383-25-9
• Molecular Formula: C₁₃H₁₉N
• Molecular Weight: 189.2967
• Mol File: 4383-25-9.mol
• Article Data: 197

Chemical Properties

• Melting Point: 149 °C
• Boiling Point: 289.8 °C at 760 mmHg
• Flash Point: 130.6 °C
• Appearance: /
• Density: 0.97 g/cm³
• Vapor Pressure: 0.00215mmHg at 25°C
• Refractive Index: 1.536
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 10.05±0.20(Predicted)
• CAS DataBase Reference: N-BENZYLCYCLOHEXYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-BENZYLCYCLOHEXYLAMINE(4383-25-9)
• EPA Substance Registry System: N-BENZYLCYCLOHEXYLAMINE(4383-25-9)

Safety Data

• Hazardous Substances Data: 4383-25-9(Hazardous Substances Data)

Usage

General Description

N-BENZYLCYCLOHEXYLAMINE is a chemical compound that belongs to the class of secondary amines and contains a benzyl group and a cyclohexyl group. It is used in the synthesis of pharmaceuticals and acts as a ligand in catalysis reactions. N-BENZYLCYCLOHEXYLAMINE has a wide range of applications, including in the production of organic solvents, corrosion inhibitors, and in the development of new materials. It is considered to be a versatile building block for the synthesis of various organic compounds and plays a crucial role in the field of organic chemistry. Additionally, it is important to handle N-BENZYLCYCLOHEXYLAMINE with care, as it may be hazardous and requires proper safety precautions in its handling and use.

InChI:InChI=1/C13H19N/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1,3-4,7-8,13-14H,2,5-6,9-11H2

Upstream product

• 2211-66-7 N-phenyl(methylidene)cyclohexanamine 
• 108-91-8 cyclohexylamine 
• 100-52-7 benzaldehyde 
• 64-18-6 formic acid 
• 108-94-1 cyclohexanone 
• 140-11-4 Benzyl acetate 
• 6281-14-7 1,3,5-tricyclohexyl-[1,3,5]triazinane 
• 100-39-0 benzyl bromide 
• 100-46-9 benzylamine 
• 108-93-0 cyclohexanol 
• 100-47-0 benzonitrile 
• 1426958-19-1 N-benzyl-N-pinacolborylcyclohexylamine 
• 98-88-4 benzoyl chloride 
• 27845-53-0 (E)-N-cyclohexyl-1-phenylmethanimine 

Downstream Products

• 92744-64-4 benzyl-cyclohexyl-dithiocarbamic acid 
• 55246-39-4 C₁₄H₁₈ClNO 
• 14256-72-5 N-Benzyl-N-cyclohexyl-aethylendiamin 
• 78822-59-0 N-benzyl-N-cyclohexylbenzenesulfinamide 

Relevant articles and documents

T-shaped (D)2–A–π–A type sensitizers incorporating indoloquinoxaline and triphenylamine for organic dye-sensitized solar cells

Four novel T-shaped metal-free organic sensitizers QX22–25 based on triphenylamine and indoloquinoxaline have been successfully designed and synthesized as a (D)2–A–π–A type structure. These dye sensitizers have two triphenylamine donors attach

Sulfated polyborate: A dual catalyst for the reductive amination of aldehydes and ketones by NaBH4

An efficient, quick, and environment-friendly one-pot reductive amination of aldehydes or ketones was developed. In ethanol at 70 °C, a imination catalyzed by sulfated polyborate and further reduced by sodium borohydride yields various amines. The present method has many significant benefits, including a shorter reaction time, excellent yields, and a hassle-free, straightforward experimental process. The reaction has a wide range of applications due to its flexibility, including secondary amine for reductive amination.

Silver/manganese dioxide nanorod catalyzed hydrogen-borrowing reactions and tert-butyl ester synthesis

Silver/manganese dioxide (Ag@MnO2) nanorods are synthesized and characterized by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray powder diffraction, and X-ray photoelectron spectroscopy. It was discovered that Ag@MnO2 nanorods can realize hydrogen-borrowing reactions in high yields and are also effective for the synthesis of tert-butyl esters from aryl cyanides and tert-butyl hydroperoxide in a short period of time. Mechanistic experiments revealed that this catalytic system acts as a Lewis acid in hydrogen-borrowing reactions, while the synthesis of tert-butyl esters occurs through a radical pathway. This is the first report on the excellent catalytic activity of Ag@MnO2 nanorods as a catalyst.