24613-65-8

Basic information

• Product Name: 1,9-DIIODONONANE
• Synonyms: 1,9-diiodo-nonan;Nonamethylene diiodide;1,9-DIIODONONANE;1,9-Diodononane
• CAS NO: 24613-65-8
• Molecular Formula: C₉H₁₈I₂
• Molecular Weight: 380.05
• EINECS: 246-355-7
• Product Categories: Iodine Compounds
• Mol File: 24613-65-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 325.3°C (estimate)
• Flash Point: 139 °C
• Appearance: /
• Density: 1.7903 (rough estimate)
• Vapor Pressure: 0.000778mmHg at 25°C
• Refractive Index: 1.4827 (estimate)
• Storage Temp.: Refrigerator, Under inert atmosphere
• Solubility: Acetone (Slightly), Chloroform (Soluble)
• CAS DataBase Reference: 1,9-DIIODONONANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,9-DIIODONONANE(24613-65-8)
• EPA Substance Registry System: 1,9-DIIODONONANE(24613-65-8)

Safety Data

• Hazardous Substances Data: 24613-65-8(Hazardous Substances Data)

Usage

Uses

1,9-Diiodononane can be used for antiviral and anticancer optimization studies of DNA-binding marine natural product aaptamine.

InChI:InChI=1/C9H18I2/c10-8-6-4-2-1-3-5-7-9-11/h1-9H2

Upstream product

• 3937-56-2 1,9-Nonanediol 
• 4549-33-1 1,9-Dibromononane 
• 858190-48-4 1-ethoxy-9-(2-methoxy-phenoxy)-non-3-yne 
• 100248-51-9 1-(5-bromo-pentyloxy)-2-methoxy-benzene 
• 821-99-8 1,9-dichlorononane 
• 860397-51-9 1-ethoxy-9-(2-methoxy-phenoxy)-nonane 
• 22543-29-9 undecanedioic acid diethyl ester 
• 1852-04-6 undecanedioic acid 
• 111-24-0 1,5-dibromo-pentane 

Relevant articles and documents

Highly Selective Radical Monoreduction of Dihalides Confined to a Dynamic Supramolecular Host

Reduction of alkyl dihalide guests (2–5 and 7) with trialkylsilanes (R3SiH) was performed in water-soluble host 1 to investigate the effects of confinement on fast radical reactions (k≥103 m?1 s?1). High selectivity (>95 %) for mono-reduced products was observed for primary and secondary dihalide guests under mild conditions. The results highlight the importance of host–guest complexation rates to modulate the product selectivity in radical reactions.