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CS-W001157 4
Total: USD 88.00

9-Phenylcarbazole

  • CAS No. 1150-62-5

  • Cat. No. CS-0018847
  • Purity≥98%
  • MDL No.MFCD00004965

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

9-Phenylcarbazole|CS-0018847

Structure of 1150-62-5

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General Information

  • CAS No. 1150-62-5
  • Cat. No. CS-0018847
  • Purity ≥98%
  • MDL No. MFCD00004965
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₈H₁₃N
  • Molecular Weight 243.31
  • Synonym(s) 9-Phenyl-9H-carbazole; N-Phenylcarbazole; N-PHENYLCARBAZOLE HYDROCHLORIDE
  • SMILES N1(C2=CC=CC=C2)C3=C(C4=C1C=CC=C4)C=CC=C3

Description

18:1 PE MCC is a maleimide-functionalized thiol-reactive lipid with a phosphoethanolamine linked to two oleic acid tails and a maleimide group. For research purposes only.

Synthesis

  • Route1
    • In-stock
      Iodobenzene|CS-W008603
      591-50-4
    • null|null
      86-74-8
    • ~97%
    • In-stock
      9-Phenylcarbazole|CS-0018847
      1150-62-5

    References

    • Kwon, Jae Kwan; Cho, Joong Hyun; Ryu, Young-Sil; Oh, Se Hwan; Yum, Eul Kgun Tetrahedron, 2011 , vol. 67, # 26 p. 4820 - 4825
  • Route2
    • null|null
      108-86-1
    • null|null
      86-74-8
    • ~99%
    • In-stock
      9-Phenylcarbazole|CS-0018847
      1150-62-5

    References

    • TOSOH CORPORATION Patent: US2007/282111 A1, 2007 ; Location in patent: Page/Page column 3; 4 ;
  • Route3
    • null|null
      122-39-4
    • null|null
      583-53-9
    • ~93%
    • In-stock
      9-Phenylcarbazole|CS-0018847
      1150-62-5

    References

    • Ackermann, Lutz; Althammer, Andreas; Mayer, Peter Synthesis, 2009 , # 20 p. 3493 - 3503

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS07
Signal Word : Danger
UN#: 1759
Class : 8
Packing Group : Ⅲ
Hazard Statements : H315-H318-H335-H413
Precautionary Statements : P261-P264-P271-P273-P280-P302+P352-P304+P340-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   4.93
  • LogP   4.7837
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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