(+)-Trans-limonene1,2-epoxide
Modify Date: 2024-01-09 00:21:50
(+)-Trans-limonene1,2-epoxide structure
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Common Name | (+)-Trans-limonene1,2-epoxide | ||
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| CAS Number | 6909-30-4 | Molecular Weight | 152.23300 | |
| Density | 0.930 g/mL at 20ºC(lit.) | Boiling Point | N/A | |
| Molecular Formula | C10H16O | Melting Point | N/A | |
| MSDS | USA | Flash Point | 65ºC | |
| Name | (4R)-limonene 1α,2α-epoxide |
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| Synonym | More Synonyms |
| Density | 0.930 g/mL at 20ºC(lit.) |
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| Molecular Formula | C10H16O |
| Molecular Weight | 152.23300 |
| Flash Point | 65ºC |
| Exact Mass | 152.12000 |
| PSA | 12.53000 |
| LogP | 2.52010 |
| Index of Refraction | n20/D 1.466 |
| Storage condition | 2-8°C |
| Personal Protective Equipment | Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
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| Hazard Codes | F |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2932999099 |
| Precursor 0 | |
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| DownStream 1 | |
CAS#:22972-51-6| HS Code | 2932999099 |
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| Summary | 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Catalytic mechanism of limonene epoxide hydrolase, a theoretical study.
J. Am. Chem. Soc. 127(41) , 14339-47, (2005) The catalytic mechanism of limonene epoxide hydrolase (LEH) was investigated theoretically using the density functional theory method B3LYP. LEH is part of a novel limonene degradation pathway found i... |
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QM/MM study of the mechanism of enzymatic limonene 1,2-epoxide hydrolysis.
Biochim. Biophys. Acta 1824(2) , 263-8, (2012) Limonene 1,2-epoxide hydrolase (LEH) is completely different from those of classic epoxide hydrolases (EHs) which catalyze the hydrolysis of epoxides to vicinal diols. A novel concerted general acid c... |
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Total synthesis of (+)-cymbodiacetal: a re-evaluation of the biomimetic route.
J. Org. Chem. 75(24) , 8465-70, (2010) A total synthesis of (+)-cymbodiacetal (1) has been completed from (R)-(+)-limonene oxide using a hetero-Diels-Alder cycloaddition as a key step. The key Diels-Alder cycloaddition proceeds with endo-s... |
| (1S,2R,4R)-4-Isopropenyl-1-methyl-1-cyclohexene 1,2-epoxide |
| D-LIMONENE 1,2-EPOXIDE |
| (1S,2R,4R)-limonene 1,2-oxide |
| (1S,4R)-1,2-Epoxy-p-menth-8-ene |
| (1R,4S)-trans-limonene oxide |
| (4R)-limonene 1alpha,2alpha-epoxide |
| (+)-trans-Limonene oxide |
| (1S,2R,4R)-limonene-1,2-epoxide |
| (+)-trans-p-Mentha-1,8-diene 1,2-epoxide |
| (+)-trans-Limonene 1,2-epoxide |
| (1S,2R,4R)-trans-1,2-limonene epoxide |
| (1S,2R)-1,2-epoxy-p-menth-8-ene |
| (1R,3R,6S)-6-methyl-3-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptane |
| 2a2g |
| trans-d-Limonene oxide |
| limonene oxide |
| LEO |