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Description
TCI C4166 4277-34-3 Cyclooct-4-enol is a chemical compound widely used in organic laboratory reactions. As a fundamental building block in the synthesis of complex molecules, it plays a crucial role in the development of both heterocyclic and non-heterocyclic compounds. This compound is particularly valued for its versatility and reactivity, making it an essential component in various synthetic pathways. Its unique structure and functional groups enable it to participate in a wide range of chemical transformations, contributing to the advancement of chemical research and development.
The properties of Cyclooct-4-enol that make it a preferred choice include its cyclic structure with a double bond and a hydroxyl group, which enhance its reactivity in chemical reactions. These characteristics allow it to be a suitable precursor in reactions such as ozonolysis, hydroboration, and substitution reactions. The compound's ability to undergo ring-opening or substitution reactions further expands its utility in synthetic chemistry. Its stability and reactivity make it an ideal choice for researchers seeking reliable and efficient chemical intermediates.
In Indonesian laboratories, Cyclooct-4-enol is commonly used in organic chemistry research, especially in the synthesis of pharmaceutical compounds and industrial chemicals. Its availability and effectiveness in various reactions make it a popular choice among researchers. This compound supports the development of new drugs and materials, contributing to both academic and industrial chemical innovation. Its role in laboratory settings is essential for advancing chemical knowledge and practical applications.
Laboratory Applications
Synthesis of heterocyclic compounds for the development of new pharmaceuticals, as Cyclooct-4-enol provides a versatile starting point for ring formation and functional group modification.
Ozonolysis reactions in the study of molecular reactivity, due to its ability to undergo cleavage under controlled conditions, offering insights into reaction mechanisms.
Hydroboration reactions in organic synthesis, where Cyclooct-4-enol serves as a reactive intermediate for the formation of alcohols and other derivatives.
Ring-opening reactions in the synthesis of complex molecules, leveraging its cyclic structure for controlled chemical transformations.
Substitution reactions in the preparation of functionalized compounds, as its hydroxyl group facilitates substitution under various reaction conditions.
Specifications
Brand: TCI
CAS number: 4277-34-3
Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes: Available in various quantities as per supplier specifications
Physical form: Liquid
Storage note: Store in a cool, dry place away from light and incompatible materials
Handling and Storage
Cyclooct-4-enol should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances such as strong oxidizers or acids. Regular monitoring of storage conditions is essential to maintain the compound's integrity and ensure safe laboratory practices.
