Benzopinacolone
Benzopinacolone (2,2,2-Triphenylacetophenone; 1,2,2,2-Tetraphenylethanone) can be synthesized when benzopinacol reacts with acids of moderate strength, causing the pinacol rearrangement. Benzopinacolone can undergo ring-opening rearrangement via appropriate epoxides reacting with acids[1].
Product Specifications
CAS Number
466-37-5
Product Name Alternative
2,2,2-Triphenylacetophenone; 1,2,2,2-Tetraphenylethanone
UNSPSC
12352005
Hazard Statement
H302-H315-H319-H335
Target
Biochemical Assay Reagents
Related Pathways
Others
Field of Research
Others
Smiles
C1=CC=C(C=C1)C(=O)C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
Molecular Formula
C26H20O
Molecular Weight
348.44
Precautions
P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
References & Citations
[1]Douglas A. Klumpp, et al. Preparation of Condensed Aromatics by Superacidic Dehydrative Cyclization of Aryl Pinacols and Epoxides1a. J. Org. Chem. 1997, 62, 19, 6666–6671.
Shipping Conditions
Room temperature
Scientific Category
Reference compound2
Clinical Information
No Development Reported
Available Sizes
Frequently Asked Questions
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