Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C28H30O3 |
| Molecular Weight | 414.536 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3
InChI
InChIKey=TWAOKHHZKFMFMD-UHFFFAOYSA-N
InChI=1S/C28H30O3/c1-3-5-11-21(4-2)20-31-28(30)26-15-10-9-14-25(26)27(29)24-18-16-23(17-19-24)22-12-7-6-8-13-22/h6-10,12-19,21H,3-5,11,20H2,1-2H3
| Molecular Formula | C28H30O3 |
| Molecular Weight | 414.536 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionSources: http://www.google.ch/patents/US4668505
Sources: http://www.google.ch/patents/US4668505
2-Ethylhexyl-4-phenyl-benzophenone carbonate (Eusolex 3573) is a component of sunscreen and possesses of ultraviolet A (UV-A) absorbing properties.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: ultraviolet A Sources: http://patents.com/us-4837019.html |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: http://patents.com/us-4837019.html |
Preventing | Eusolex 3573 Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.google.ch/patents/US4668505
Unknown
Route of Administration:
Topical
| Substance Class |
Chemical
Created
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Mon Mar 31 18:06:18 GMT 2025
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93NOD9WBCS
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C851
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