Introduction：Basic information about CAS 4683-50-5|3-Methoxy-2-cyclopenten-1-one, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | 3-Methoxy-2-cyclopenten-1-one |
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| CAS Number | 4683-50-5 | Molecular Weight | 112.127 |
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| Density | 1.1±0.1 g/cm3 | Boiling Point | 214.9±29.0 °C at 760 mmHg |
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| Molecular Formula | C6H8O2 | Melting Point | 49-53ºC(lit.) |
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| MSDS | ChineseUSA | Flash Point | 96.5±17.8 °C |
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Names
| Name | 3-methoxycyclopent-2-en-1-one |
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| Synonym | More Synonyms |
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Chemical & Physical Properties
| Density | 1.1±0.1 g/cm3 |
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| Boiling Point | 214.9±29.0 °C at 760 mmHg |
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| Melting Point | 49-53ºC(lit.) |
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| Molecular Formula | C6H8O2 |
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| Molecular Weight | 112.127 |
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| Flash Point | 96.5±17.8 °C |
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| Exact Mass | 112.052429 |
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| PSA | 26.30000 |
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| LogP | -0.04 |
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| Vapour Pressure | 0.2±0.4 mmHg at 25°C |
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| Index of Refraction | 1.467 |
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| InChIKey | DTWCFCILAJVNPE-UHFFFAOYSA-N |
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| SMILES | COC1=CC(=O)CC1 |
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| RIDADR | NONH for all modes of transport |
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| HS Code | 2914509090 |
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Customs
| 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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Articles4
More Articles
| Synthesis and structure-activity relationship of cyclopentenone oximes as novel inhibitors of the production of tumor necrosis factor-α. Bioorg. Med. Chem. Lett. 24(13) , 2807-10, (2014) 3-Alkyl-2-aryl-2-cyclopenten-1-one oxime derivatives (1) were studied as a novel class of inhibitors of tumor necrosis factor α (TNF-α) with regard to synthesis and in vitro SAR inhibition of TNF-α. T... | |
| Stereoselective α-quaternization of 3-methoxycycloalk-2-enones via 1,4-diastereoinduction of alkoxy dienolates. J. Org. Chem. 77(2) , 1202-7, (2012) The alkylation of dienolates generated from 3-methoxycycloalk-2-enones having a 3'-hydroxyl alkenyl chain provides the corresponding quaternized cycloalkenones in a highly diastereoselective manner. T... | |
| Expanding the scope of asymmetric electrophilic atom-transfer reactions: titanium- and ruthenium-catalyzed hydroxylation of beta-ketoesters. Proc. Natl. Acad. Sci. U. S. A. 101(16) , 5810-4, (2004) The enantioselective formation of a quaternary stereogenic center coinciding with a hydroxylation process is a very rare reaction from a homogeneous catalysis point of view. Indeed, to our knowledge, ... | |
Synonyms
| 3-Methoxycyclopent-2-enone |
| 3-Methoxy-2-cyclopenten-1-one |
| 1-methoxy-2-cyclopenten-1-one |
| 3-methoxy-cyclopent-2-en-1-one |
| 3-methoxycyclopent-2-ene-1-one |
| MFCD00192267 |
| 2-Cyclopenten-1-one, 3-methoxy- |
| 3-Methoxycyclopent-2-en-1-one |
| 3-methoxy-2-cyclopentene-1-one |
