7289-51-2

Basic information

• Product Name: 1-METHOXYNONANE
• Synonyms: 1-METHOXYNONANE;Methylnonyl ether
• CAS NO: 7289-51-2
• Molecular Formula: C₁₀H₂₂O
• Molecular Weight: 158.28
• Product Categories: Anisoles, Alkyloxy Compounds & Phenylacetates
• Mol File: 7289-51-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: -28.46°C (estimate)
• Boiling Point: 183.4°C (estimate)
• Flash Point: 61.6°C
• Appearance: /
• Density: 0.7945 (estimate)
• Vapor Pressure: 0.6mmHg at 25°C
• Refractive Index: 1.4063 (estimate)
• CAS DataBase Reference: 1-METHOXYNONANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHOXYNONANE(7289-51-2)
• EPA Substance Registry System: 1-METHOXYNONANE(7289-51-2)

Safety Data

• Hazardous Substances Data: 7289-51-2(Hazardous Substances Data)

Usage

General Description

1-Methoxynonane, also known by its chemical formula C10H22O, is a colorless liquid with a faint, floral odor. It is commonly used as a fragrance ingredient in various consumer products and is also used in the synthesis of other chemicals. 1-Methoxynonane is classified as a synthetic organic compound and is not considered to be a hazardous substance. It is relatively stable under normal conditions, but can react with strong oxidizing agents. The primary route of exposure to 1-Methoxynonane is through inhalation, and it is important to handle and store this chemical in a well-ventilated area to avoid exposure. Due to its low volatility and low water solubility, it is not considered to be highly toxic or harmful to the environment.

InChI:InChI=1/C10H22O/c1-3-4-5-6-7-8-9-10-11-2/h3-10H2,1-2H3

Upstream product

• 18824-63-0 1,1-dimethoxynonane 
• 67-56-1 methanol 
• 124-19-6 nonan-1-al 
• 111-66-0 oct-1-ene 
• 143-08-8 nonyl alcohol 
• 1070-00-4 trioctylaluminum 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 143-08-8 nonyl alcohol 
• 74-88-4 methyl iodide 
• 124-19-6 nonan-1-al 

Relevant articles and documents

Production of Alcohols from Olefins via One-Pot Tandem Hydroformylation-Acetalization-Hydrogenolysis over Bifunctional Catalyst Merging RuIII-P Complex and RuIII Lewis Acid

A novel three-step tandem hydroformylation-acetalization-hydrogenolysis was first proposed to produce alcohols (derivatives) from olefins, and the developed unique Ru(III)-complex [Ru(III)-L2] ligated by the ionic diphosphine (L2) proved efficient toward this tandem reaction. In Ru(III)-L2, the strong π-acceptor nature of L2 guaranteed Ru-center remaining in +3 valence state without redox reaction. Hence, Ru(III)-L2 was able to behave as a bifunctional catalyst merging RuIII-P complex and RuIII Lewis acid, which acted not only as a transition metal catalyst responsible for hydroformylation of olefins and hydrogenolysis of (hemi)acetals but also as a Ru3+ Lewis acid in charge of acetalization of aldehydes [to form (hemi)acetals]. The easily performed acetalization served as a bridge step to get through the pathway from aldehydes to alcohols instead of the direct hydrogenation.

Synthesis and Reactivity of 2-Oxidodiaryliodonium Zwitterions

The direct synthesis of three new 2-oxidoaryliodonium zwitterions from phenols and aryliodine(III) bistrifluoroacetate and their reaction with nucleophiles and electrophiles are reported.Especially noteworthy is the reactivity of 2-methoxy-3,5-dinitrophenyl(phenyl)iodonium tetrafluoroborate (15) which is hydrolysed by water and solvolysed by alcohols at room temperature.