α-Methylstyrene dimer

  • CasNo:6144-04-3
  • purity:99%
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What is the α-Methylstyrene dimer ?

α-Methylstyrene dimer is , while it's Molecular Formula is C18H20. Used in Polymer Production Industry:
α-Methylstyrene dimer is used as a monomer for the production of thermoplastic polymers, such as polystyrene and other copolymers, due to its ability to form stable polymer chains that exhibit desirable properties like flexibility and durability.
Used in Chemical Synthesis:
α-Methylstyrene dimer serves as a chemical intermediate in the synthesis of various organic compounds, contributing to the development of new chemical products and materials with specific applications in different industries.
Used in Environmental Management:
Given its potential as an environmental pollutant, α-Methylstyrene dimer is also involved in the development of strategies and technologies for its safe handling, storage, and disposal to minimize its impact on the environment and human health.

What is the CAS number for α-Methylstyrene dimer ?

The CAS number of α-Methylstyrene dimer is 6144-04-3.

More information of α-Methylstyrene dimer 6144-04-3 are:

CAS?Number

6144-04-3

Molecular Formula

C18H20

Molecular Weight

236.3514

Density

g/cm3

Boiling Point

162.5°Cat760mmHg

Flash Point

45.6°C

PSA

0.00000

LogP

5.43940

What is α-Methylstyrene dimer (6144-04-3) used for?

α-Methylstyrene dimer, also known as 1,3-Diphenyl-1-Butene, is a chemical compound formed by the dimerization of α-methylstyrene. It is a colorless to pale yellow liquid with a pungent, fruity odor and is used as a monomer for the production of thermoplastic polymers and as a chemical intermediate in the synthesis of various organic compounds. However, it is considered a potential environmental pollutant and may cause irritation to the skin, eyes, and respiratory system, necessitating proper handling and storage.

InChI:InChI=1/2C9H10/c2*1-8(2)9-6-4-3-5-7-9/h2*3-7H,1H2,2H3

Articles related to α-Methylstyrene dimer:

Article

Source

Noble-metal-free deoxygenation of epoxides: Titanium dioxide as a photocatalytically regenerable electron-transfer catalyst

Shiraishi, Yasuhiro,Hirakawa, Hiroaki,Togawa, Yoshiki,Hirai, Takayuki

, p. 1642 - 1649 (2014)

Site-Selective Acceptorless Dehydrogenation of Aliphatics Enabled by Organophotoredox/Cobalt Dual Catalysis

Zhou, Min-Jie,Zhang, Lei,Liu, Guixia,Xu, Chen,Huang, Zheng

supporting information, p. 16470 - 16485 (2021/10/20)

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