Tetrafenilciclopentadienona, 98 %, Thermo Scientific Chemicals

Name: Tetrafenilciclopentadienona, 98 %, Thermo Scientific Chemicals
SKU: A12756.06
Price: 32.80 EUR

CAS: 479-33-4 | C29H20O | 384.478 g/mol

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5 g

25 g

100 g

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Número de catálogo A12756.06

también denominado A12756-06

Precio (EUR)

32,80

Each

Cantidad:

5 g

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Precio (EUR)

32,80

Each

Identificadores químicos

CAS479-33-4

IUPAC Nametetraphenylcyclopenta-2,4-dien-1-one

Molecular FormulaC29H20O

InChI KeyPLGPSDNOLCVGSS-UHFFFAOYSA-N

SMILESO=C1C(=C(C(=C1C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1

Especificaciones Specification Sheet

Hoja de especificaciones

Appearance (Color)Black

FormCrystals or powder or crystalline powder

Assay (HPLC)≥97.5%

Melting Point (clear melt)216.0-222.0?C

It is an easily made building block for many organic and organometallic compounds.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
Se trata de un elemento básico de fácil fabricación para muchos compuestos orgánicos y organometálicos.

Solubilidad
Soluble en benceno. Insoluble en agua.

Notas
Almacenar en lugar fresco y seco en un recipiente cerrado herméticamente. Con buena ventilación. Almacénese lejos de los agentes oxidantes.

RUO – Research Use Only

General References:

L. Zhi; J. Wu; J. Li; M. Stepputat; U. Kolb; K. Müllen. Diels-Alder Reactions of Tetraphenylcyclopentadienones in Nanochannels: Fabrication of Nanotubes from Hyperbranched Polyphenylenes. Advanced Materials. 2005, 17(12), 1492-1496.
John W. Elder. Microwave Synthesis of Tetraphenylcyclopentadienone and Dimethyl Tetraphenylphthalate. J. Chem. Educ. 1994, 71(6), A142.
Reaction with alkynes is accompanied by extrusion of CO to give the aromatic system; see, e.g. (diphenylacetylene): Org. Synth. Coll., 5, 604 (1973). Reaction with maleimide in nitrobenzene leads directly to the aromatized product: J. Heterocycl. Chem., 9, 1251 (1972).