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  3. Drug Intermediate
  4. Triphenylene

Triphenylene is a highly symmetrical polycyclic aromatic hydrocarbon. Triphenylene shows no carcinogenic activity in mouse skin application experiments. Triphenylene can be used as a drug intermediate for the synthesis of triphenyl polycyclic aromatic hydrocarbons (PAHs).

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Triphenylene

Triphenylene Chemical Structure

CAS No. : 217-59-4

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Other Forms of Triphenylene:

Triphenylene Related Antibodies

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Description

Triphenylene is a highly symmetrical polycyclic aromatic hydrocarbon. Triphenylene shows no carcinogenic activity in mouse skin application experiments. Triphenylene can be used as a drug intermediate for the synthesis of triphenyl polycyclic aromatic hydrocarbons (PAHs)[1][2].

Masse moléculaire

228.29

Formule

C18H12
CAS No.
Appearance

Solid

SMILES

C=1C=CC=2C(C1)=C3C=CC=CC3=C4C=CC=CC24
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Store at room temperature 3 years

In solvent -80°C 2 years
-20°C 1 year
Pureté et documentation

Purity: 99.30%

SDS (619 KB)

COA (255 KB) HNMR (119 KB) RP-HPLC (94 KB)

Instruction de manipulation (2659 KB)
Références
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Triphenylene Related Classifications

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Triphenylene217-59-4Drug IntermediateDrug IintermediateCyclization strategyPhotoinduced synthesisSynthetic methodsTransition metal catalysisTriphenylene derivativesInhibitorinhibitorinhibit

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