1,3-Dioxol-2-one, 4,5-diphenyl-


Chemical Name: 1,3-Dioxol-2-one, 4,5-diphenyl-
CAS Number: 21240-34-6
Product Number: AG003KIK(AGN-PC-0JLXOR)
Synonyms:
MDL No:
Molecular Formula: C15H10O3
Molecular Weight: 238.2381

Identification/Properties


Properties
MP:
1-75 °C
BP:
366.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 4,5-Diphenyl-1,3-dioxol-2-one, also known as benzilideneacetone, is a versatile molecule widely used in chemical synthesis. Its unique structure, featuring a dioxolane ring system flanked by two phenyl groups, imparts special reactivity and functionality that make it valuable for various synthetic applications.One key use of 4,5-Diphenyl-1,3-dioxol-2-one is as a building block in the synthesis of complex organic molecules. Its carbonyl groups can undergo a variety of reactions, such as nucleophilic additions, enolate formations, and condensations, allowing for the efficient construction of intricate structures. Additionally, the presence of the phenyl groups provides opportunities for further functionalization and diversification of the molecule.Furthermore, 4,5-Diphenyl-1,3-dioxol-2-one is a common starting material for the preparation of chiral ligands and catalysts in asymmetric synthesis. By modifying the structure around the dioxolane ring, chemists can create tailored molecules that exhibit high enantioselectivity in catalytic reactions, enabling the efficient production of enantiomerically pure compounds.Overall, the versatile reactivity and structural features of 4,5-Diphenyl-1,3-dioxol-2-one make it a valuable tool in organic synthesis, particularly in the construction of complex molecules and the development of chiral catalysts.