Interesting facts
Interesting Facts About Cyclohexa-1,4-diene
Cyclohexa-1,4-diene is a fascinating compound due to its unique structure and properties that capture the attention of chemists. This cyclic alkene features a six-membered carbon ring with two double bonds located at the 1 and 4 positions. Here are some intriguing aspects of this compound:
- Conjugated System: The alternating single and double bonds in cyclohexa-1,4-diene form a conjugated system, which contributes to its stability and reactivity. This property allows the compound to exhibit interesting electronic characteristics, such as absorption of UV light.
- Isomerism: Cyclohexa-1,4-diene can exist in different isomeric forms. The arrangement of double bonds and their spatial orientation (cis/trans) introduces a variety of structural possibilities, leading to differing properties and reactions.
- Applications in Organic Synthesis: This compound serves as a useful intermediate in organic synthesis. For chemists, it acts as a building block for synthesizing complex molecules used in pharmaceuticals and materials science.
- Reactivity: The presence of the double bonds makes cyclohexa-1,4-diene reactive under certain conditions. For instance, it can undergo Diels-Alder reactions, which is a crucial reaction in organic chemistry for forming cyclic compounds.
- Historical Significance: The study of cycloalkenes like cyclohexa-1,4-diene has provided insights into the foundations of organic chemistry and the nature of chemical bonding, helping scientists understand the principles of resonance and stability in organic compounds.
As demonstrated, cyclohexa-1,4-diene is not just a simple hydrocarbon; it is a compound that plays a significant role in various chemical processes and applications. Its study continues to yield valuable information on chemical reactivity and compound synthesis.
Synonyms
1,4-CYCLOHEXADIENE
Cyclohexa-1,4-diene
EINECS 211-043-1
UNII-0F8Z5909QZ
0F8Z5909QZ
DTXSID0060854
CHEBI:37611
DTXCID6043547
3,5,2'-trihydroxy-6,7-(2'',2''-dimethylcromene)-8-(3''',3'''-dimethylallyl)-dihydroflavonol
3,5-dihydroxy-2-(2-hydroxy-phenyl)-8,8-dimethyl-10-(3-methyl-but-2-enyl)-2,3-dihydro-8h-pyrano(3,2-g)chromen-4-one
3,5-dihydroxy-2-(2-hydroxy-phenyl)-8,8-dimethyl-10-(3-methyl-but-2-enyl)-2,3-dihydro-8h-pyrano[3,2-g]chromen-4-one
inchi=1/c25h26o6/c1-13(2)9-10-16-22-15(11-12-25(3,4)31-22)19(27)18-20(28)21(29)24(30-23(16)18)14-7-5-6-8-17(14)26/h5-9,11-12,21,24,26-27,29h,10h2,1-4h3/t21-,24+/m0/s
inchi=1/c6h8/c1-2-4-6-5-3-1/h1-2,5-6h,3-4h
rel-(7r,8r)-5,7-dihydroxy-8-(2-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-en-1-yl)-7,8-dihydro-2h,6h-pyrano(3,2-g)chromen-6-one
rel-(7r,8r)-5,7-dihydroxy-8-(2-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-en-1-yl)-7,8-dihydro-2h,6h-pyrano[3,2-g]chromen-6-one
uvjhqyioxkwhfd-uhfffaoysa-n
628-41-1
1,4-Dihydrobenzene
1,4-Cyclohexanediene
MFCD00001535
1,4-Cyclohexadiene, 97%
1,4 cyclohexadiene
AKOS015902349
BP-31161
1,4-Cyclohexadiene (stabilized with BHT)
NS00035192
1,4-Cyclohexadiene, purum, >=97.0% (GC)
D89254
EN300-112479
Q161523
1,4-Cyclohexadiene ~0.1% hydroquinone as stabilizer
Solubility of Cyclohexa-1,4-diene
Cyclohexa-1,4-diene, with the chemical formula C6H8, presents unique solubility characteristics due to its structural configuration. This compound is classified as an unsaturated cyclic hydrocarbon, which affects its interactions with solvents.
Key Aspects of Solubility:
In conclusion, while cyclohexa-1,4-diene may not be soluble in water, its solubility in non-polar organic solvents makes it a suitable candidate for various chemical applications. As stated in solubility principles: "Like dissolves like." Therefore, it is essential to consider the nature of the solvent when working with this compound.