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Tetraphenylcyclopentadienone, 98%, Thermo Scientific Chemicals
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Catalog number A12756.14
also known as A12756-14
Price (USD)/ Each
97.65
Online exclusive
108.00 Save 10.35 (10%)
-
Quantity:
25 g
Price (USD)/ Each
97.65
Online exclusive
108.00 Save 10.35 (10%)
Tetraphenylcyclopentadienone, 98%, Thermo Scientific Chemicals
Catalog numberA12756.14
Price (USD)/ Each
97.65
Online exclusive
108.00 Save 10.35 (10%)
-
Chemical Identifiers
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
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Specifications
Specification Sheet
Specification SheetAppearance (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.
Applications
It is an easily made building block for many organic and organometallic compounds.
Solubility
Soluble in Benzene. Insoluble in water.
Notes
Store in cool dry place in tightly closed container. With good ventilation. Store away from oxidizing agent.
It is an easily made building block for many organic and organometallic compounds.
Solubility
Soluble in Benzene. Insoluble in water.
Notes
Store in cool dry place in tightly closed container. With good ventilation. Store away from oxidizing agent.
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).