Weight | 310.393 g/mol |
---|---|
Formula | C20H22O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 5 |
Avobenzone (70356-09-1)
parsol 1789 · parsol-1789 · 4-tert-butyl-4'-methoxydibenzoylmethane
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- Polymorphism and Reversible Mechanochromic Luminescence for Solid-State Difluoroboron Avobenzone (Journal of the American Chemical Society, 2010)
- Photostabilization of Butyl methoxydibenzoylmethane (Avobenzone) and Ethylhexyl methoxycinnamate by Bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb S), a New UV Broadband Filter (Photochemistry and Photobiology, 2001)
- Unexpected Photolysis of the Sunscreen Octinoxate in the Presence of the Sunscreen Avobenzone (Photochemistry and Photobiology, 2004)
- The Relationship of Solid-State Plasticity to Mechanochromic Luminescence in Difluoroboron Avobenzone Polymorphs (Advanced Functional Materials, 2013)
- Photostability of the sunscreening agent 4-tert-butyl-4 -methoxydibenzoylmethane (avobenzone) in solvents of different polarity and proticity (Journal of Photochemistry and Photobiology A-chemistry, 2008)
- A Blocked Diketo Form of Avobenzone: Photostability, Photosensitizing Properties and Triplet Quenching by a Triazinederived UVBfilter (Photochemistry and Photobiology, 2009)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - parsol 1789
- parsol-1789
- 4-tert-butyl-4'-methoxydibenzoylmethane
-
SMILESCC(C)(C)C1=CC=C(C=C1)C(=O)CC(=O)C2=CC=C(C=C2)OC
-
InChIKeyXNEFYCZVKIDDMS-UHFFFAOYSA-N
- Pubchem - Avobenzone
- Wikipedia - avobenzone
Avobenzone (trade names Parsol 1789, Milestab 1789, Eusolex 9020, Escalol 517, Neo Heliopan 357 and others, INCI Butyl Methoxydibenzoylmethane) is an oil-soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays.
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Synthesis
ANISOLE
+
Reactant
(Friedel-Crafts acylation)
4-Methoxyphenylboronic acid
+
Reactant
(Suzuki)
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