CAS 592-48-3

1,3-Hexadiene

Description:

1,3-Hexadiene is a linear diene hydrocarbon with the molecular formula C6H10. It features two double bonds located at the first and third carbon atoms in its chain, which contributes to its reactivity and makes it a valuable intermediate in organic synthesis. This compound is a colorless liquid at room temperature and has a characteristic odor. It is insoluble in water but soluble in organic solvents such as ethanol and ether. 1,3-Hexadiene is flammable and should be handled with care, as it can form explosive mixtures with air. Its reactivity allows it to participate in various chemical reactions, including polymerization, where it can be used to produce synthetic rubber and other materials. Additionally, it can undergo addition reactions with electrophiles, making it useful in the synthesis of more complex organic compounds. Due to its unsaturated nature, it is also a subject of study in the field of polymer chemistry and materials science.

Formula: C₆H₁₀

InChI: InChI=1/C6H10/c1-3-5-6-4-2/h3,5-6H,1,4H2,2H3/b6-5-

InChI key: InChIKey=AHAREKHAZNPPMI-UHFFFAOYSA-N

SMILES: C(=CC=C)CC

Synonyms:

• (3E)-hexa-1,3-diene
• (3Z)-hexa-1,3-diene
• 1,3-Hexadiene,mixture of cis and trans
• Hexa-1,3-Diene
• Hexadiene
• 1-Ethyl-1,3-butadiene
• 1,3-Hexadiene
• (3E)-1,3-Hexadiene
• 1-Ethyl-1．3-butadiene
• cis,trans-hexa-1,3-diene
• 1,3-HEXADIENE, 96%, MIXTURE OF CIS AND TRANS
• Hexadiene-1，3
• TRANS-1,3-HEXADIENE
• 1,3-Hexadiene,c&t
• trans-1,3-Hexadiene (stabilized with TBC)
• (E)-1,3-Hexadiene
• 1,3-Hexadiene(c,t)
• C2H5CH=CHCH=CH2

1,3-Hexadiene

CAS: 592-48-3

1,3-Hexadiene is a cyclopentadienyl that is used in the production of polymers and plastics. It is produced by the reaction of n-hexane with solid-phase synthesis. The reaction mechanism involves the formation of an activated complex, which then reacts with styrene. This produces a c-h bond between two carbons, which can be converted to a double bond by adding one proton and electron to each carbon. The kinetic studies show that activation energy for this process is 42 kJ/mol. Functional theory predicts that 1,3-hexadiene will react with an electron donor such as methanol or ethanol to produce methylcyclohexane or ethylcyclohexane respectively.

Formula: C₆H₁₀

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 82.14 g/mol

Ref: 3D-FH03126