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CS-W001157 4
Total: USD 88.00

Benzo[b]naphtho[2,1-d]thiophene

  • CAS No. 239-35-0

  • Cat. No. CS-0535351
  • Purity≥98%
  • MDL No.MFCD00010043

*For research and further manufacturing use only, not for direct human use.

Benzo[b]naphtho[2,1-d]thiophene|CS-0535351

Structure of 239-35-0

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General Information

  • CAS No. 239-35-0
  • Cat. No. CS-0535351
  • Purity ≥98%
  • MDL No. MFCD00010043
  • Storage Sealed in dry,2-8℃
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₁₀S
  • Molecular Weight 234.32
  • Synonym(s) 1,2-Benzobiphenylene Sulphide
  • SMILES C1=CC=C2C(=C1)C=CC3=C2SC4=CC=CC=C34

Description

1,2-benzodiphenylene sulfide is a rare constituent of coal tar. Photodeoxygenation of 1,2-benzodiphenylene sulfoxide, generates an intermediate capable of oxidizing the solvent benzene to phenol. Liquid-phase photolysis of 1,2-benzodiphenylene sulfide to generate atomic oxygen [O(3P)] or an equivalent active oxygen species has been reported.1,2-Benzodiphenylene sulfide has been used in direct screening of sediment samples for polycyclic aromatic hydrocarbons by flow manifold coupled on-line to a fluorimetric detector.

Synthesis

  • Route1
    • null|null
      696-59-3
    • null|null
      234-41-3
    • ~91%
    • Benzo[b]naphtho[2,1-d]thiophene|CS-0535351
      239-35-0

    References

    • Rafiq, Settu Muhamad; Sivasakthikumaran, Ramakrishnan; Mohanakrishnan, Arasambattu K. Organic Letters, 2014 , vol. 16, # 10 p. 2720 - 2723
  • Route2

    References

    • Universal Display Corporation Patent: US2011/266526 A1, 2011 ;
  • Route3
    • null|null
      1146542-57-5
    • ~42%
    • Benzo[b]naphtho[2,1-d]thiophene|CS-0535351
      239-35-0

    References

    • Li, Ang; DeSchepper, Daniel J.; Klumpp, Douglas A. Tetrahedron Letters, 2009 , vol. 50, # 17 p. 1924 - 1927

Safety Information

Download SDS
GHS Pictogram : N/A
GHS No : N/A
Signal Word : N/A
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

Quality Control

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Computational Chemistry Data

  • TPSA   0
  • LogP   5.2077
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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