Cyclopentenone structure
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Common Name | Cyclopentenone | ||
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CAS Number | 930-30-3 | Molecular Weight | 82.10 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 136.0±0.0 °C at 760 mmHg | |
Molecular Formula | C5H6O | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 42.2±0.0 °C | |
Symbol |
GHS02 |
Signal Word | Warning |
Use of CyclopentenoneCyclopent-2-enone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 2-Cyclopenten-1-one |
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Synonym | More Synonyms |
Description | Cyclopent-2-enone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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Related Catalog |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 136.0±0.0 °C at 760 mmHg |
Molecular Formula | C5H6O |
Molecular Weight | 82.10 |
Flash Point | 42.2±0.0 °C |
Exact Mass | 82.041862 |
PSA | 17.07000 |
LogP | -0.05 |
Vapour Pressure | 7.5±0.2 mmHg at 25°C |
Index of Refraction | 1.492 |
Storage condition | 2-8°C |
Water Solubility | almost insoluble |
Symbol |
GHS02 |
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Signal Word | Warning |
Hazard Statements | H226 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R10;R22;R36/37/38 |
Safety Phrases | S16-S36-S36/37/39 |
RIDADR | UN 1224 3/PG 3 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 3 |
HS Code | 2914299000 |
Precursor 0 | |
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DownStream 10 | |
HS Code | 2914299000 |
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Summary | 2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
The cyclopentenone prostaglandin 15d-PGJ2 inhibits the NLRP1 and NLRP3 inflammasomes.
J. Immunol. 194(6) , 2776-85, (2015) Inflammasomes are cytosolic protein complexes that respond to diverse danger signals by activating caspase-1. The sensor components of the inflammasome, often proteins of the nucleotide-binding oligom... |
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Enantioselective synthesis of 4-heterosubstituted cyclopentenones.
J. Org. Chem. 78(8) , 4202-6, (2013) Racemic 4-hydroxycyclopentenone, readily derived from furfuryl alcohol, can be transformed via its O-Boc derivative to 4-acyloxy, 4-aryloxy-, 4-amino-, or 4-thio-substituted cyclopentenones with high ... |
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Sinularones A-I, new cyclopentenone and butenolide derivatives from a marine soft coral Sinularia sp. and their antifouling activity.
Mar. Drugs 10(6) , 1331-44, (2012) Nine new compounds, namely sinularones A-I (1-9), characterized as cyclopentenone and butenolide-type analogues, were isolated from a soft coral Sinularia sp., together with a known butenolide (10). T... |
2-Cyclopentenone |
cyclopent-2-en-1-one |
EINECS 213-213-0 |
3-Cyclopenten-2-one |
Cyclopentenone |
MFCD00001401 |
2-Cyclopenten-1-one |