CAS 3212-75-7

2-Cycloocten-1-ol

Description:

2-Cycloocten-1-ol is a cyclic organic compound characterized by its unique structure, which features a cyclooctene ring with a hydroxyl (-OH) group attached at the first carbon position. This compound is classified as an alcohol due to the presence of the hydroxyl functional group. It is typically a colorless to pale yellow liquid with a distinctive odor. The presence of the double bond in the cyclooctene ring contributes to its reactivity, making it susceptible to various chemical reactions, such as oxidation and polymerization. 2-Cycloocten-1-ol is soluble in organic solvents and exhibits moderate solubility in water. Its applications may include use in organic synthesis, as a building block for more complex molecules, and potentially in the fragrance industry due to its aromatic properties. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Overall, 2-Cycloocten-1-ol is an interesting compound with potential utility in various chemical applications.

Formula: C₈H₁₄O

InChI: InChI=1S/C8H14O/c9-8-6-4-2-1-3-5-7-8/h4,6,8-9H,1-3,5,7H2

InChI key: InChIKey=UJZBDMYKNUWDPM-UHFFFAOYSA-N

SMILES: OC1CCCCCC=C1

Synonyms:

• (2Z)-2-Cycloocten-1-ol
• (2Z)-cyclooct-2-en-1-ol
• (Z)-2-Cycloocten-1-ol
• (Z)-Cyclooct-2-enol
• 2-Cycloocten-1-ol
• 2-Cyclooctenol
• 3-Hydroxycyclooctene
• NSC 105771
• cis-2-Cyclooctenol

2-Cycloocten-1-ol

CAS: 3212-75-7

2-Cycloocten-1-ol

Purity: 98%

Molecular weight: 126.2g/mol

Ref: 54-OR1001113

Cyclooct-2-enol

CAS: 3212-75-7

Purity: 95%

Molecular weight: 126.198997497559

Ref: 10-F867415

(Z)-Cyclooct-2-enol

Controlled Product

CAS: 3212-75-7

Formula: C₈H₁₄O

Color and Shape: Neat

Molecular weight: 126.196

Ref: TR-Z701708

(2Z)-Cyclooct-2-en-1-ol

CAS: 3212-75-7

(2Z)-Cyclooct-2-en-1-ol is a catalytic oxidant that is used in the epoxidation of cyclic and acyclic olefins. It has been shown to interact with hydroxy groups and it can be used to cleave bonds. The reaction between (2Z) -cyclooct-2-en-1-ol and lithium diisopropylamide (LDA) gives an acceleration in the rate of the reaction due to steric interactions. The kinetic data for this reaction have been obtained by measuring the rates of hydrogen abstraction from (2Z)-cyclooct-2-en-1-ol using deuterium gas.

Formula: C₈H₁₄O

Purity: Min. 95%

Molecular weight: 126.2 g/mol

Ref: 3D-DAA21275