79419-72-0

Basic information

• Product Name: N-cyclohexylbutane-1,4-diamine
• Synonyms: N-cyclohexylbutane-1,4-diamine;N-(4-Aminobutyl)-N-cyclohexylamine
• CAS NO: 79419-72-0
• Molecular Formula: C₁₀H₂₂N₂
• Molecular Weight: 170.29508
• EINECS: 279-154-8
• Mol File: 79419-72-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 259.8°C at 760 mmHg
• Flash Point: 127.8°C
• Appearance: /
• Density: 0.9g/cm³
• Vapor Pressure: 0.0127mmHg at 25°C
• Refractive Index: 1.483
• PKA: 11.02±0.20(Predicted)
• CAS DataBase Reference: N-cyclohexylbutane-1,4-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-cyclohexylbutane-1,4-diamine(79419-72-0)
• EPA Substance Registry System: N-cyclohexylbutane-1,4-diamine(79419-72-0)

Safety Data

• Hazardous Substances Data: 79419-72-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H22N2/c11-8-4-5-9-12-10-6-2-1-3-7-10/h10,12H,1-9,11H2

Upstream product

• 108-94-1 cyclohexanone 
• 110-60-1 1,4-diaminobutane 
• 108-91-8 cyclohexylamine 
• 77516-53-1 N-cyclohexyl-2-nitrobenzenesulfonamide 
• 1020957-41-8 4-(cyclohexylamino)butanenitrile 

Relevant articles and documents

Chemical Synthesis and Biological Effect on Xylem Formation of Xylemin and Its Analogues

Xylemin (6) and its designed structural analogues 18–23, N-(4-aminobutyl)alkylamines, were synthesized by 2-nitrobenzenesulfonamide (Ns) strategy. Investigation of the improved synthesis of 20–23 resulted in the development of one-step synthesis of these analogues from the commercially available corresponding ketones. Biological assessment of the synthetic molecules elucidated that xylemin (6) and the analogue N-(4-aminobutyl)cyclopentylamine (21) promoted the expression level of thermospermine synthase ACAULIS5 (ACL5) and enhanced xylem formation. In addition, xylemin (6) was found to significantly promote lateral root formation, whereas xylemin analogues 18–23 including 21 did not. These results indicate that the analogue 21 has the potential as a novel inhibitor of thermospermine synthesis to work specifically in xylem differentiation.