4,4'-(ethene-1,2-diyl)bis(2,6-di-tert-butylcyclohexa-2,4-dien-1-one)
$300.00
CAS No.: 809-73-4
Catalog No.: 195077
Purity: 95%
MF: C30H44O2
MW: 436.68
Storage: 2-8 degree Celsius
SMILES: C(=CC=1C=C(C(C(C1)C(C)(C)C)=O)C(C)(C)C)C=1C=C(C(C(C1)C(C)(C)C)=O)C(C)(C)C
Catalog No.: 195077
Purity: 95%
MF: C30H44O2
MW: 436.68
Storage: 2-8 degree Celsius
SMILES: C(=CC=1C=C(C(C(C1)C(C)(C)C)=O)C(C)(C)C)C=1C=C(C(C(C1)C(C)(C)C)=O)C(C)(C)C
4,4'-(ethene-1,2-diyl)bis(2,6-di-tert-butylcyclohexa-2,4-dien-1-one); CAS No.: 809-73-4; 4,4'-(ethene-1,2-diyl)bis(2,6-di-tert-butylcyclohexa-2,4-dien-1-one). PROPERTIES: 4,4'-(ethene-1,2-diyl)bis(2,6-di-tert-butylcyclohexa-2,4-dien-1-one) appears as a white to off-white crystalline powder with a slight odor. Its molecular formula is C28H36O4, corresponding to a molecular weight of approximately 440.6 g/mol. The compound exhibits a melting point in the range of 180-183 C and demonstrates moderate solubility in common organic solvents such as toluene, hexane, and diethyl ether while being sparingly soluble in water. It is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: 4,4'-(ethene-1,2-diyl)bis(2,6-di-tert-butylcyclohexa-2,4-dien-1-one) functions as a specialized intermediate in the synthesis of antioxidant additives used in polymers and lubricants. Its bis-tert-butylcyclohexadienone structure provides excellent radical scavenging properties, making it valuable for preventing oxidative degradation in various materials (Journal of Applied Polymer Science). In pharmaceutical research, 4,4'-(ethene-1,2-diyl)bis(2,6-di-tert-butylcyclohexa-2,4-dien-1-one) serves as a building block for creating bioactive molecules, including certain anticancer agents and enzyme inhibitors, where its conjugated dienone system enables selective targeting of biological pathways (Bioorganic & Medicinal Chemistry Letters). Additionally, the compound finds application in the development of fluorescent probes for bioimaging, where its dienone moieties provide strong fluorescence quantum yield and its bis-structure allows for selective labeling of biological targets (Analytical Chemistry). It is also employed in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings (Pest Management Science).
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