1(2H)-Naphthalenone, octahydro-
Modify Date: 2024-01-02 18:49:34
1(2H)-Naphthalenone, octahydro- structure
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Common Name | 1(2H)-Naphthalenone, octahydro- | ||
|---|---|---|---|---|
| CAS Number | 4832-16-0 | Molecular Weight | 152.23300 | |
| Density | 0.986 g/mL at 25ºC(lit.) | Boiling Point | 73-75ºC1 mm Hg(lit.) | |
| Molecular Formula | C10H16O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 190 °F | |
| Name | 3,4,4a,5,6,7,8,8a-octahydro-2H-naphthalen-1-one |
|---|---|
| Synonym | More Synonyms |
| Density | 0.986 g/mL at 25ºC(lit.) |
|---|---|
| Boiling Point | 73-75ºC1 mm Hg(lit.) |
| Molecular Formula | C10H16O |
| Molecular Weight | 152.23300 |
| Flash Point | 190 °F |
| Exact Mass | 152.12000 |
| PSA | 17.07000 |
| LogP | 2.54580 |
| Index of Refraction | n20/D 1.492(lit.) |
| Precursor 10 | |
|---|---|
| DownStream 5 | |
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Stereochemistry of catalysis by the ketoreductase activity in the first extension module of the erythromycin polyketide synthase.
Biochemistry 41(8) , 2719-26, (2002) Multiple ketoreductase activities play a crucial role in establishing the stereochemistry of the products of modular polyketide synthases (PKSs), but there has been little systematic scrutiny of catal... |
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The metabolism of the isomeric decalones.
Biochem. J. 100(2) , 393-402, (1966) 1. The metabolism of (+/-)-cis-1-, (+/-)-trans-1-, (+/-)-cis-2- and (+/-)-trans-2-decalone in the rabbit has been investigated. 2. (+/-)-cis-2- and (+/-)-trans-2-Decalone were both reduced to racemic ... |
| hexahydroketonaphthalene |
| dihydronaphthalenone |
| hexahydronaphthalenone |
| 1-DECALONE (CIS-TRANS) |
| octahydro-1(2H)-naphthalenone |
| BICYCLO(4.4.0)-2-DECANONE |
| dihydronaphthalen-4-one |
| Bicyclo[4.4.0]decane-2-one |
| bicyclo[4.4.0]decan-2-one |
| Mixtureofcis-/trans-isomeres |
| MFCD00001697 |
| Einecs 225-410-9 |
| ketotetrahydronaphthalene |
| bicyclo(4.4.0)decan-1-one |
| DECAHYDRO-1-NAPHTHALENONE |
| Decahydronaphthalen-1-one |