5876-87-9

Basic information

• Product Name: 1,11-DODECADIENE
• Synonyms: 1,11-DODECADIENE;1,11-DODECADIENE 99+%;1,6-Bis(2-propenyl)hexane;dodeca-1,11-diene
• CAS NO: 5876-87-9
• Molecular Formula: C₁₂H₂₂
• Molecular Weight: 166.3
• Mol File: 5876-87-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 207 °C
• Flash Point: 69.3°C
• Appearance: /
• Density: 0.77
• Vapor Pressure: 0.305mmHg at 25°C
• Refractive Index: 1.4370-1.4400
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Ethyl Acetate (Slightly)
• CAS DataBase Reference: 1,11-DODECADIENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,11-DODECADIENE(5876-87-9)
• EPA Substance Registry System: 1,11-DODECADIENE(5876-87-9)

Safety Data

• Hazardous Substances Data: 5876-87-9(Hazardous Substances Data)

Usage

General Description

1,11-Dodecadiene is a chemical compound with the molecular formula C12H22. It is a colorless liquid with a faint odor, and is commonly used as an intermediate in the production of various chemicals such as perfumes and pharmaceuticals. Its structure consists of a chain of 12 carbon atoms with two double bonds between the 1st and 11th carbon atoms. 1,11-Dodecadiene is primarily utilized in the production of polymers and elastomers, as well as in the synthesis of specialty chemicals. It is important in the manufacturing of various consumer products and industrial applications due to its unique properties and versatility. However, it should be handled with care and proper safety precautions due to its flammable nature.

InChI:InChI=1/C12H22/c1-3-5-7-9-11-12-10-8-6-4-2/h3-4H,1-2,5-12H2

Upstream product

• 2695-47-8 6-Bromo-1-hexene 
• 629-03-8 1 ,6-dibromohexane 
• 106-95-6 allyl bromide 
• 563-47-3 3-Chloro-2-methylpropene 

Downstream Products

• 45037-67-0 decanedial 
• 5578-80-3 ω-oxydecanocarboxylic acid 
• 1338212-77-3 C₃₆H₆₂ 
• 1239513-50-8 C₂₄H₄₂ 
• 3344-70-5 1,12-dibromododecane 
• 99828-63-4 dodec-11-ene bromide 
• 5009-33-6 1-dodecen-11-one 
• 7029-09-6 2,11-dodecadione 
• 111-20-6 1,10-decanedioic acid 
• 5675-51-4 1,12-dodecandiol 
• 3313-59-5 2-heptylcyclohexanone 
• 82001-53-4 12-mercaptododecanoic acid 
• 73367-80-3 12-bromododecanoic acid 

Relevant articles and documents

Concerning the Mechanism of Grignard Reagent Formation. Evidence for Radical Escape and Return to the Surface of Magnesium

A study of the mechanism of formation of Grignard reagents using alkyl halide radical probes has been conducted.The effects of activation of the magnesium, temperature, concentration of the alkyl halide, magnesium to alkyl halide ratio, magnesium purity, the nature of the alkyl group, the nature of the halide group, and solvent (viscosity and basicity) on the formation of Grignard reagent were studied.The data obtained were used to test the earlier report by Garst that alkyl radicals, generated in the reaction of an alkyl halide with magnesium, diffuse freely into the solvent phase and return to the magnesium surface to form Grignard reagent.In this study cyclizable radical probes and radical traps were employed to study the extent to which radicals leave and return to the surface of magnesium to form Grignard reagent.In the particular system reported here, the data indicate that ca.25percent of the Grignard reagent is formed from radicals that diffuse into the solvent phase and than return to the magnesium surface to form Grignard reagent.