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| 1 4 4A 8A-TETRAHYDRO-ENDO-1 4-METHANO- Basic information |
| Product Name: | 1 4 4A 8A-TETRAHYDRO-ENDO-1 4-METHANO- | | Synonyms: | 1 4 4A 8A-TETRAHYDRO-ENDO-1 4-METHANO-;1,4,4A,8A-tetrahydro-endo-1,4-methano-naphthalene;RHENIUM(IV) OXIDE, 99.7%;Nsc196244;1,4-Methanonaphthalene-5,8-dione, 1,4,4a,8a-tetrahydro-, (1R,4S,4aR,8aS)-rel-;1,4,4a,8a-Tetrahydro-endo-1,4-methanonaphthalene-5,8-dione 98% | | CAS: | 51175-59-8 | | MF: | C11H10O2 | | MW: | 174.2 | | EINECS: | | Product Categories: | Building Blocks;C11 to C12;C11 to C12;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Carbonyl Compounds;Ketones | | Mol File: | 51175-59-8.mol |
| 1 4 4A 8A-TETRAHYDRO-ENDO-1 4-METHANO- Chemical Properties |
| Melting point | 77-79 °C (lit.) | | Boiling point | 317.6±42.0 °C(Predicted) | | density | 1.273±0.06 g/cm3(Predicted) |
| 1 4 4A 8A-TETRAHYDRO-ENDO-1 4-METHANO- Usage And Synthesis |
| Uses | 1,4,4a,8a-Tetrahydro-endo-1,4-methanonaphthalene-5,8-dione may be used in the synthesis of pentacyclo[5.4.0.02,6.03,10.05,9]undecane-8,11-dione (the ′cage′ compound) via the intramolecular [2+2]-photocycloaddition reaction. | | General Description | 1,4,4a,8a-Tetrahydro-endo-1,4-methanonaphthalene-5,8-dione can be prepared by Diels-Alder reaction of cyclopentadiene and 1,4-benzoquinone. |
| 1 4 4A 8A-TETRAHYDRO-ENDO-1 4-METHANO- Preparation Products And Raw materials |
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