![]() Tropinone structure
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Common Name | Tropinone | ||
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CAS Number | 532-24-1 | Molecular Weight | 139.195 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 217.1±0.0 °C at 760 mmHg | |
Molecular Formula | C8H13NO | Melting Point | 40-44 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 90.0±0.0 °C |
Use of TropinoneTropinone, an alkaloid, acts as a synthetic intermediate to Atropine[1]. |
Name | tropinone |
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Synonym | More Synonyms |
Description | Tropinone, an alkaloid, acts as a synthetic intermediate to Atropine[1]. |
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Related Catalog | |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 217.1±0.0 °C at 760 mmHg |
Melting Point | 40-44 °C(lit.) |
Molecular Formula | C8H13NO |
Molecular Weight | 139.195 |
Flash Point | 90.0±0.0 °C |
Exact Mass | 139.099716 |
PSA | 20.31000 |
LogP | 0.07 |
Vapour Pressure | 0.1±0.4 mmHg at 25°C |
Index of Refraction | 1.505 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S23-S24/25-S36/37/39-S26-S22 |
RIDADR | 1544 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 6.1 |
HS Code | 2933990090 |
Precursor 9 | |
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DownStream 9 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Toxicity of field bindweed (Convolvulus arvensis) to mice.
Vet. Hum. Toxicol. 37(5) , 452-4, (1995) The effects of feeding high and low doses of field bindweed (Convolvulus arvensis) to mice were investigated. Bindweed contains several alkaloids, including pseudotropine, and lesser amounts of tropin... |
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Synthesis and applications of masked oxo-sulfinamides in asymmetric synthesis.
Org. Biomol. Chem. 10(26) , 5021-31, (2012) This short perspective reports on the synthesis and applications of a class of chiral amino carbonyl compounds, masked oxo-sulfinamides where the amine is protected with an N-sulfinyl moiety and the c... |
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Biosynthesis of calystegines: 15N NMR and kinetics of formation in root cultures of Calystegia sepium.
Phytochemistry 62(3) , 325-32, (2003) Calystegines are nortropane alkaloids bearing between three and five hydroxyl groups in various positions. [15N]Tropinone was administered to root cultures of Calystegia sepium and the incorporation i... |
Tropanon |
N-methyl-3-tropanone |
8-azabicyclo[3.2.1]octan-3-one, 8-methyl-, (1S,5S)- |
8-Methyl-8-azabicyclo[3.2.1]-3-octanone |
3-tropinone |
tropan-3-one |
(1S,5S)-8-Methyl-8-azabicyclo[3.2.1]octan-3-one |
Tropinone |
EINECS 208-530-6 |
Tropinon |
Tropanone |
3-Tropanone |
8-Azabicyclo[3.2.1]octan-3-one, 8-methyl-, (1R,5S)- |
(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-one |
1αH,5αH-tropan-3-one |
8-methyl-8-aza-bicyclo[3.2.1]octan-3-one |
MFCD00005549 |
1αH,5αH-Tropan-3-one (8CI) |
TROPIONONE |
8-methyl-8-azabicyclo[3.2.1]oct-3-one |
8-methyl-8-azabicyclo[3.2.1]octane-3-one |