CAS 30282-14-5

2-hydroxycyclohexanone dimer

Description:

2-Hydroxycyclohexanone dimer, with the CAS number 30282-14-5, is an organic compound characterized by its dimeric structure formed from the condensation of two molecules of 2-hydroxycyclohexanone. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, reflecting its polar functional groups. The presence of the hydroxyl (-OH) group contributes to its potential reactivity, particularly in hydrogen bonding and as a site for further chemical modifications. The dimerization process can influence its physical properties, such as melting point and boiling point, compared to its monomeric counterpart. Additionally, 2-hydroxycyclohexanone dimer may exhibit interesting chemical behavior, including potential applications in polymer chemistry or as an intermediate in organic synthesis. Its stability and reactivity can be affected by environmental factors such as temperature and pH, making it a subject of interest in both industrial and academic research settings. Safety data should be consulted for handling and usage, as with all chemical substances.

Formula: C₆H₁₀O₂

InChI: InChI=1/C12H20O4/c13-11-7-3-1-5-9(11)15-12(14)8-4-2-6-10(12)16-11/h9-10,13-14H,1-8H2

InChI key: InChIKey=OLLWHBLCQGPTMZ-UHFFFAOYSA-N

SMILES: OC12C(OC3(O)C(O1)CCCC3)CCCC2

Synonyms:

• 1,2,3,4,5a,6,7,8,9,10a-Decahydrodibenzo-p-dioxin-4a,9a-diol
• 2-Hydroxycyclohexan-1-one dimer
• Adipoin dimer
• Cyclohexanone, 2-hydroxy-, dimer
• Dibenzo-p-dioxin-4a,9a(2H,5aH)-diol, octahydro-
• Dibenzo[b,e][1,4]dioxin-4a,9a(2H,5aH)-diol, octahydro-
• Nsc 117392
• Octahydrodibenzo[b,e][1,4]dioxin-4a,9a(2H,5aH)-diol
• octahydrooxanthrene-4a,9a(2H,5aH)-diol
• AKOS 92461
• 2-Hydroxycyclohexanone dimer,Adipoin
• ADIPOIN
• 2-HYDROXYCYCLOHEXANONE, DIMER, 90+%

2-Hydroxycyclohexanone dimer, 90+%

CAS: 30282-14-5

It is a reactant involved in the synthesis of substrates for tin tetrachloride mediated fragmentation to produce ynones and ynoates, tandem oxidation coupling reactions with diamines, asymmetric allylic alkylation of enolates and formate reduction of allylic carbonates for polypropionate systems. Th

Formula: C₆H₁₀O₂

Purity: 90+%

Color and Shape: Powder, White to pale cream

Molecular weight: 114.14

Ref: 02-H27199

2-Hydroxycyclohexanone dimer

CAS: 30282-14-5

Formula: C₁₂H₂₀O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 228.2848

Ref: IN-DA003HFH

2-Hydroxycyclohexanone dimer

CAS: 30282-14-5

2-Hydroxycyclohexanone dimer is a molecule that has a hydroxyl group, a carbon source, and two fatty acid chains. It can be used as an organic solvent. 2-Hydroxycyclohexanone dimer can be synthesized by reacting benzaldehyde with cyclohexanol in the presence of potassium hydroxide. The reaction mechanism for this synthesis is base formation followed by the cleavage of the ester bond to produce 2-hydroxycyclohexanone and cyclohexanol. 2-Hydroxycyclohexanone dimer has been shown to react with oxygen to form peroxide and hydrogen peroxide which are both oxidizing agents. This compound also has redox potentials that range from -0.77 V to -1.06 V, making it useful for electrochemical reactions in fuel cells or batteries.

Formula: C₆H₁₀O₂

Purity: 90%Nmr

Molecular weight: 228.28 g/mol

Ref: 3D-FBA28214