1,9-Decadiene - ≥95%(GC) , CAS No.1647-16-1

CAS: 1647-16-1 Cat. No.: D1521027 Formula: C₁₀H₁₈ Peso molecolare: 138.25 Numero EC: 216-711-6

GRADE & PURITY ≥95%(GC)

Storage

Room temperature

Shipped In

Normal

Panoramica

1,9-Decadiene acts as comonomer and undergoes acyclic diene metathesis (ADMET) copolymerization with 1, 5-hexadiene to form random linear polybutadiene -polyoctenamer copolymers. It undergoes ADMET copolymerization with divinyltetraethoxydisiloxane to yield siloxylene-vinylene-alkenylene copolymer.
1,9-Decadiene was used in synthesis and characterization of new telechelic polyoctenamers prepared by ADMET polymerization using Grubbs catalyst.

Specifications

Specifiche e purezza

≥95%(GC)

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥95%(GC)

Nomi e identificatori

• Sorrisi canonici: C=CCCCCCCC=C
• IUPAC Name: deca-1,9-diene
• InChIKey: NLDGJRWPPOSWLC-UHFFFAOYSA-N
• INCHI: 1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-4H,1-2,5-10H2
• Isomeri SMILES: C=CCCCCCCC=C
• WGK Germania: 3
• Numero UN: 3295
• Gruppo di imballaggio: III
• Peso molecolare: 138.25
• Reaxy-Rn: 1697870
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697870&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbons
    • Classe Unsaturated hydrocarbons
      • Subclass Olefins
        • Level5 Acyclic olefins
          • Level6 Alkadienes

• Kingdom: Organic compounds
• Superclass: Hydrocarbons
• Classe: Unsaturated hydrocarbons
• Subclass: Olefins
• Intermediate Tree Nodes: Acyclic olefins
• Direct Parent: Alkadienes
• Alternative Parents: Unsaturated aliphatic hydrocarbons
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkadiene - Unsaturated aliphatic hydrocarbon - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alkadienes. These are acyclic hydrocarbons that contain exactly two carbon-to-carbon double bonds.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Solubilità: It is soluble in organic solvents.
• Indice di rifrazione: 1.4320 to 1.4340
• Punto di infiammabilità (°F): 105.8 °F
• Punto di infiammabilità (°C): 41°C
• Punto di ebollizione (°C): 165°C
• Peso molecolare: 138.250 g/mol
• XLogP3: 5.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 7
• Exact Mass: 138.141 Da
• Monoisotopic Mass: 138.141 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 70.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Bao Jingxian, Fan Yonghui, Zhang Shuyi, Zhong Liangshu, Wu Minghong, Sun Yuhan.  (2019)  Hydrofunctionalization of Olefins to Higher Aliphatic Alcohols via Visible-Light Photocatalytic Coupling.  CATALYSIS LETTERS,  149  (6): (1651-1659).  [PMID:] [10.1007/s10562-019-02737-3]