1,6-Heptadiene is an organic compound classified as a diene, characterized by the presence of two double bonds within its seven-carbon chain. Its molecular formula is C7H12, indicating that it is an unsaturated hydrocarbon. The structure features double bonds between the first and second, as well as the sixth and seventh carbon atoms, which contributes to its reactivity and potential for polymerization. 1,6-Heptadiene is a colorless liquid at room temperature and has a characteristic odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic nature. This compound is primarily used in organic synthesis and as an intermediate in the production of various chemicals, including polymers and fine chemicals. Due to the presence of multiple double bonds, it can undergo various chemical reactions, such as addition reactions, making it a valuable building block in synthetic organic chemistry. Safety precautions should be taken when handling 1,6-heptadiene, as it is flammable and may pose health risks upon exposure.

1,6-Heptadiene

1,6-Heptadiene is a reactive monomer that is used in the synthesis of polymers. It can be synthesized by copolymerization with styrene and ethylene. 1,6-Heptadiene reacts readily with chloride and pyridine to form a pyridine complex. The vinyl groups on the cyclopentane ring react with nucleophiles such as amines to form five-membered rings. This monomer has been shown to be stereoselective, reacting preferentially with one enantiomer of an alcohol rather than the other. 1,6-Heptadiene has been used for structural analysis by NMR spectroscopy and is also useful for ligand design.

CAS 3070-53-9: 1,6-Heptadiene

1,6-Heptadiene

Ref: 3B-H0564

1,6-Heptadiene

Ref: 3D-FH158001