2473-01-0

Basic information

• Product Name: 1-CHLORONONANE
• Synonyms: NONYL CHLORIDE;N-NONYL CHLORIDE;1-CHLORONONANE;1-Chlornonan;1-chloro-nonan;Nonane,1-chloro-;Nonylchlorid;1-Chlorononane,98%
• CAS NO: 2473-01-0
• Molecular Formula: C₉H₁₉Cl
• Molecular Weight: 162.7
• EINECS: 219-595-5
• Product Categories: Alkyl Chlorides;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes
• Mol File: 2473-01-0.mol
• Article Data: 14

Chemical Properties

• Melting Point: -39.4°C
• Boiling Point: 202-204 °C(lit.)
• Flash Point: 166 °F
• Appearance: /
• Density: 0.87 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.394mmHg at 25°C
• Refractive Index: n20/D 1.436(lit.)
• Storage Temp.: Store below +30°C.
• BRN: 1733625
• CAS DataBase Reference: 1-CHLORONONANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-CHLORONONANE(2473-01-0)
• EPA Substance Registry System: 1-CHLORONONANE(2473-01-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 2473-01-0(Hazardous Substances Data)

Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

1-Chlorononane has been used in the synthesis of 2-bromo[1-14C]1-decanal, affinity labeling probe for the aliphatic aldehyde site of Vibrio harveyi luciferase.

InChI:InChI=1/C9H19Cl/c1-2-3-4-5-6-7-8-9-10/h2-9H2,1H3

Upstream product

• 111-84-2 nonane 
• 143-08-8 nonyl alcohol 
• 4282-42-2 1-iodononane 
• 68506-47-8 chloro-dinonyl-aluminium 
• 124-11-8 non-1-ene 
• 112-20-9 n-Nonylamin 
• 82394-19-2 1,4-dinonylpiperazine 
• 6212-33-5 2-(4-Chlorophenyl)glycine 
• 7719-09-7 thionyl chloride 
• 71-43-2 benzene 
• 10026-13-8 phosphorus pentachloride 
• 7719-12-2 phosphorus trichloride 
• 110-86-1 pyridine 
• 91-22-5 quinoline 

Downstream Products

• 101425-55-2 benzyl-nonyl sulfide 
• 1081-77-2 n-nonylbenzene 
• 53657-08-2 N-nonylimidazole 
• 16979-32-1 2-(1-nonyloxy)-1-ethanol 
• 124-11-8 non-1-ene 
• 1975-78-6 [1-¹³C₁]-decanenitrile 
• 25727-94-0 4-decylmorpholine 
• 112-31-2 caprinaldehyde 
• 111-84-2 nonane 
• 629-50-5 Tridecane 
• 1002-69-3 decyl chloride 
• 2189-60-8 Octylbenzene 
• 7116-86-1 5,5-dimethyl-hex-1-ene 
• 36382-10-2 5,5-dimethyl-hex-2-ene 

Relevant articles and documents

METHOD FOR PRODUCING REDUCED HALIDE COMPOUND HAVING UNDERGONE REDUCTION OF CARBON-CARBON UNSATURATED BOND

A halide compound having one or more carbon-carbon unsaturated bonds is catalytically reduced with substantially no dehalogenation to produce a reduced halide compound in which at least one of the one or more unsaturated bonds is reduced. Specifically provided is a method for producing a reduced halide compound including steps of: reacting a nickel compound, a zinc compound, and a borohydride compound in a solvent to obtain a reduction catalyst; and subjecting a halide compound having one or more carbon-carbon unsaturated bonds to catalytic reduction in the presence of the reduction catalyst to reduce at least one of the one or more carbon-carbon unsaturated bonds to thereby obtain a reduced halide compound.

Copper-catalyzed cross-coupling of functionalized alkyl halides and tosylates with secondary and tertiary alkyl Grignard reagents

Added value: A copper-based method is highly efficient for the cross-coupling of alkyl electrophiles with secondary and tertiary alkyl Grignard reagents. The method is distinguished by its broad substrate scope and high functional group tolerance. Copyright