5471-56-7

Basic information

• Product Name: 1-(cyclohex-1-en-1-yl)propan-2-amine
• CAS NO: 5471-56-7
• Molecular Formula: C₉H₁₇N
• Molecular Weight: 139.238
• Mol File: 5471-56-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 206.1°C at 760 mmHg
• Flash Point: 80.2°C
• Density: 0.893g/cm³
• Vapor Pressure: 0.242mmHg at 25°C
• Refractive Index: 1.485
• CAS DataBase Reference: 1-(cyclohex-1-en-1-yl)propan-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(cyclohex-1-en-1-yl)propan-2-amine(5471-56-7)
• EPA Substance Registry System: 1-(cyclohex-1-en-1-yl)propan-2-amine(5471-56-7)

Safety Data

• Hazardous Substances Data: 5471-56-7(Hazardous Substances Data)

Usage

Structure

Contains a cyclohexene ring and a propan-2-amine group

Classification

Amine derivative

Applications

a. Organic synthesis
b. Pharmaceutical research
c. Potential use in the development of new drugs
d. Building block for the synthesis of other chemical compounds

Reactivity

Valuable for studying due to its structure and properties

Biological activity

Potential for investigation in the field of chemistry and pharmaceuticals

Upstream product

• 768-50-3 1-cyclohexenylacetone 
• 77287-34-4 formamide 
• 24826-68-4 1-(cyclohex-1-en-1-yl)propan-2-ol 
• 87143-30-4 (cyclohex-1-en-1-yl)-CH₂-CO-NH₂ 
• 18294-87-6 1-cyclohexenylacetic acid 
• 79-24-3 Nitroethane 
• 1192-88-7 1-cyclohexene-1-carboxaldehyde 

Relevant articles and documents

Catalytic Multisite-Selective Acetoxylation Reactions at sp2 vs sp3 C-H Bonds in Cyclic Olefins

The first Pd-catalyzed multisite-selective acetoxylation reactions are disclosed at an unactivated alkene sp2 C-H bond versus secondary allylic sp3 C-H bond in cyclic olefins via the modulation of directing groups. The different directing groups overcome the key challenge in differentiating C-H bonds and provide a new controlling approach for site-specific C-H activation. A wide variety of substrates are readily acetoxylated under operationally simple conditions. Mechanistic studies suggest that different Pd (IV) intermediates were involved in the multisite-selective acetoxylation reactions.