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AF83095

4277-34-3 | 5-Hydroxy-1-cyclooctene

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $8.00 $5.00 -   +
250mg 97% in stock $10.00 $7.00 -   +
1g 97% in stock $22.00 $16.00 -   +
5g 97% in stock $73.00 $52.00 -   +
10g 97% in stock $138.00 $97.00 -   +
25g 97% in stock $330.00 $231.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AF83095
Chemical Name: 5-Hydroxy-1-cyclooctene
CAS Number: 4277-34-3
Molecular Formula: C8H14O
Molecular Weight: 126.1962
MDL Number: MFCD06252442
SMILES: O[C@H]1CCCC=CCC1
NSC Number: 119487

 

Computed Properties
Complexity: 96.7  
Covalently-Bonded Unit Count: 1  
Defined Bond Stereocenter Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
Undefined Atom Stereocenter Count: 1  
XLogP3: 1.8  

 

 

Upstream Synthesis Route
  • Cyclooct-4-enol, also known as cyclooct-4-en-1-ol, is a versatile compound widely used in chemical synthesis. Its ability to undergo various chemical reactions makes it a valuable intermediate in the preparation of complex organic molecules. In organic synthesis, Cyclooct-4-enol serves as a key building block for the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary applications of Cyclooct-4-enol is in the synthesis of cyclic compounds such as cyclooctanones and cyclooctanols. Through selective functional group modifications, Cyclooct-4-enol can be transformed into a range of derivatives with diverse chemical properties. Furthermore, its unique structural features allow for the introduction of different functional groups, enabling chemists to tailor the molecule for specific reaction pathways.Cyclooct-4-enol plays a crucial role in hydrogenation reactions, where it can be hydrogenated to yield cyclooctanone or selectively oxidized to form cyclooctanoic acid. Additionally, its conjugated double bond system makes it a suitable substrate for various addition reactions, leading to the formation of ring-closing products or functionalized intermediates.Overall, Cyclooct-4-enol's versatile reactivity and synthetic potential make it an indispensable compound in the arsenal of organic chemists for the efficient construction of complex molecular structures. Its applications extend beyond basic chemical research to the synthesis of advanced materials and bioactive compounds, illustrating its significance in modern chemical synthesis.
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