• 1. Linear free-energy relationships for water/hexadec-1-ene and water/deca-1,9-diene partitions, and for permeation through lipid bilayers; comparison of permeation systems
  Michael H. Abraham,William E. Acree New J. Chem. 2012 36 1798
• 2. Response to “A critique of Abraham and Acree's correlation for deca-1,9-diene–water partition coefficients”
  Michael H. Abraham,William E. Acree,Jr. New J. Chem. 2013 37 882
• 3. A critique of Abraham and Acree’s correlation for deca-1,9-diene/water partition coefficients
  Johannes M. Nitsche,Gerald B. Kasting New J. Chem. 2013 37 283
• 4. A critique of Abraham and Acree’s correlation for deca-1,9-diene/water partition coefficients
  Johannes M. Nitsche,Gerald B. Kasting New J. Chem. 2013 37 283
• 5. Interactions of polysulfanes with components of red blood cells
  Thomas Schneider,Lalla A. Ba,Khairan Khairan,Clemens Zwergel,Nguyen Duc Bach,Ingolf Bernhardt,Wolfgang Brandt,Ludger Wessjohann,Marc Diederich,Claus Jacob Med. Chem. Commun. 2011 2 196

• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Unsaturated hydrocarbons Olefins Acyclic olefins
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Chemical Profile: CAS No. 1647-16-1 - 1,9-Decadiene

CAS No. 1647-16-1, commonly referred to as 1,9-Decadiene, is a hydrocarbon compound with the molecular formula C??H??. This compound belongs to the class of alkenes and is characterized by its two double bonds located at positions 1 and 9 of the decane chain. The structure of 1,9-Decadiene makes it a unique molecule with interesting chemical properties and potential applications in various fields.

The synthesis of 1,9-Decadiene has been a topic of interest in organic chemistry due to its structural complexity. Recent studies have explored innovative methods for its preparation, including the use of metathesis reactions and tailored catalytic systems. These advancements have not only improved the yield but also opened new avenues for its utilization in specialized chemical industries.

Diene structures, such as 1,9-Decadiene, are known for their reactivity in Diels-Alder reactions. This compound has shown promising results as a dienophile in such reactions, leading to the formation of complex ring structures with high stereochemical control. Researchers have leveraged this property to synthesize advanced materials for applications in drug delivery systems and polymer science.

In terms of physical properties, 1,9-Decadiene exhibits a low melting point and high volatility, making it suitable for certain industrial processes that require precise temperature control. Its stability under standard conditions also contributes to its desirability in large-scale manufacturing.

The application of CAS No. 1647-16-1 extends beyond traditional chemical synthesis. Recent findings suggest its potential as a precursor in the production of specialty polymers and high-performance lubricants. Its ability to form stable adducts with various reagents further enhances its utility in material science.

In conclusion, CAS No. 1647-16-1 - 1,9-Decadiene stands out as a versatile compound with significant potential across multiple disciplines. Ongoing research continues to uncover new applications and optimize its synthesis methods, solidifying its role as an essential component in modern chemistry.

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