7-Methoxy-3,4-dihydronaphthalen-2(1H)-one structure
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Common Name | 7-Methoxy-3,4-dihydronaphthalen-2(1H)-one | ||
|---|---|---|---|---|
| CAS Number | 4133-34-0 | Molecular Weight | 176.212 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 306.8±0.0 °C at 760 mmHg | |
| Molecular Formula | C11H12O2 | Melting Point | 27 - 28ºC | |
| MSDS | Chinese USA | Flash Point | 150.8±21.4 °C | |
| Name | 7-Methoxy-2-tetralone |
|---|---|
| Synonym | More Synonyms |
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 306.8±0.0 °C at 760 mmHg |
| Melting Point | 27 - 28ºC |
| Molecular Formula | C11H12O2 |
| Molecular Weight | 176.212 |
| Flash Point | 150.8±21.4 °C |
| Exact Mass | 176.083725 |
| PSA | 26.30000 |
| LogP | 1.64 |
| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
| Index of Refraction | 1.549 |
| InChIKey | XEAPZXNZOJGVCZ-UHFFFAOYSA-N |
| SMILES | COc1ccc2c(c1)CC(=O)CC2 |
| Storage condition | 0-6°C |
| Precursor 9 | |
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| DownStream 10 | |
| HS Code | 2914509090 |
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| Summary | HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
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Synthesis and dopaminergic activity of 2-substituted octahydrobenzo[f]quinolines.
J. Med. Chem. 32 , 961, (1989) A series of 2-substituted octahydrobenzo[f]quinolines has been synthesized and assayed for dopamine agonist activity. Only the compounds corresponding to the beta-rotameric conformation of dopamine sh... |
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8,9-methylenedioxybenzo[i]phenanthridines: topoisomerase I-targeting activity and cytotoxicity.
Bioorg. Med. Chem. 11(17) , 3795-3805, (2003) Substituted benzo[i]phenanthridines that have incorporated within their structure an 8,9-methylenedioxy group can exhibit topoisomerase I-targeting activity. Structure-activity studies were performed ... |
| 3,4-Dihydro-7-methoxy-2(1H)-naphthalenone |
| 3,4-dihydro-7-methoxynaphthalen-1(2H)-one |
| 7-Methoxy-3,4-dihydronaphthalen-1(2H)-one |
| EINECS 223-954-1 |
| MFCD00001730 |
| 7-Methoxy-2-tetralone |
| 1(2H)-Naphthalenone, 3,4-dihydro-7-methoxy- |
| 2(1H)-Naphthalenone, 3,4-dihydro-7-methoxy- |
| 7-methoxy-3,4-dihydro-1H-naphthalen-2-one |
| 7-Methoxy-3,4-dihydro-2(1H)-naphthalenone |
| 7-Methoxy-3,4-dihydronaphthalen-2(1H)-one |
| 7-Methoxy-3,4-dihydro-1(2H)-naphthalenone |