5,6-Dimethoxy-1-indanone structure
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Common Name | 5,6-Dimethoxy-1-indanone | ||
|---|---|---|---|---|
| CAS Number | 2107-69-9 | Molecular Weight | 192.211 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 339.7±42.0 °C at 760 mmHg | |
| Molecular Formula | C11H12O3 | Melting Point | 118-122 ºC | |
| MSDS | Chinese USA | Flash Point | 150.4±14.3 °C | |
| Name | 5,6-dimethoxy-2,3-dihydroinden-1-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 339.7±42.0 °C at 760 mmHg |
| Melting Point | 118-122 ºC |
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.211 |
| Flash Point | 150.4±14.3 °C |
| Exact Mass | 192.078644 |
| PSA | 35.53000 |
| LogP | 2.26 |
| Vapour Pressure | 0.0±0.7 mmHg at 25°C |
| Index of Refraction | 1.550 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xn: Harmful; |
| Risk Phrases | R20/21/22 |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2914509090 |
| Precursor 9 | |
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| DownStream 10 | |
| HS Code | 2914509090 |
|---|---|
| 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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Thienylhalomethylketones: Irreversible glycogen synthase kinase 3 inhibitors as useful pharmacological tools
Bioorg. Med. Chem. 17 , 6914-25, (2009) Thienylhalomethylketones, whose chemical, biological, and pharmaceutical data are here reported, are the first irreversible inhibitors of GSK-3beta described to date. Their inhibitory activity is like... |
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Ring-substituted 11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides with similar patterns of cytotoxicity to the dual topo I/II inhibitor DACA.
Bioorg. Med. Chem. 7(12) , 2801-9, (1999) A series of ring-substituted analogues of the topoisomerase inhibitor 11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides was prepared and evaluated. The compounds were prepared by Pfitzinger reaction of... |
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Inhibition of bovine viral diarrhea virus RNA synthesis by thiosemicarbazone derived from 5,6-dimethoxy-1-indanone.
J. Virol. 85(11) , 5436-45, (2011) In the present work, we described the activity of the thiosemicarbazone derived from 5,6-dimethoxy-1-indanone (TSC), which we previously characterized as a new compound that inhibits bovine viral diar... |
| 1H-Inden-1-one, 2,3-dihydro-5,6-dimethoxy- |
| 5,6-Dimethoxy-2,3-dihydro-1H-inden-1-on |
| EINECS 218-287-8 |
| MFCD00612461 |
| 5,6-Dimethoxy-indan-1-one |
| 1H-Inden-1-one,2,3-dihydro-5,6-dimethoxy |
| 5,6-dimethoxy-2,3-dihydro-1H-inden-1-one |
| 5,6-dimethoxyindan-1-one |
| 5,6-Dimethoxy-1-indanone |
| 3,4-dimethoxy-1-indanone |
| 5,6-Dimethoxyindan-1-on |
| 5,6-DIMETHOXY-2,3DIHYDRO-1H-INDEN-1-ONE |
| Donepezil Impurity 25 |