5-EXO-BENZENESELENYL-6-ENDO-CHLOROBICYCLO-[2.2.1]-HEPTANE
Compound with spectra: 2 NMR
![5-EXO-BENZENESELENYL-6-ENDO-CHLOROBICYCLO-[2.2.1]-HEPTANE](/api/compound/2jWR9wg8x5k.png?ph=true&h=300&w=458 "5-EXO-BENZENESELENYL-6-ENDO-CHLOROBICYCLO-[2.2.1]-HEPTANE")
| SpectraBase Compound ID | 2jWR9wg8x5k |
|---|---|
| InChI | InChI=1S/C13H15ClSe/c14-12-9-6-7-10(8-9)13(12)15-11-4-2-1-3-5-11/h1-5,9-10,12-13H,6-8H2/t9-,10+,12-,13-/m1/s1 |
| InChIKey | HWLZCFLBNBSXNP-LYIQGSDWSA-N |
| Mol Weight | 285.69 g/mol |
| Molecular Formula | C13H15ClSe |
| Exact Mass | 286.00275 g/mol |
| Enantiomer InChIKey | HWLZCFLBNBSXNP-LFSVMHDDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CH3OH |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- EXO-2-PHENYLSELENO-ENDO-3-CHLOROBICYCLO-[2.2.1]-HEPTANE
SYN-7-PHENYLSELENO-EXO-2-CHLOROBICYCLO-[2.2.1]-HEPTANE
2-(PHENYLSELENO)-9-OXABICYCLO-[3.3.1]-NONANE
2-(PHENYLSELENO)-9-OXABICYCLO-[4.2.1]-NONANE
FYVFDDLDXXCKBR-UBHSHLNASA-N
trans-(1-Methyl-2-phenylseleno-cyclohexyl)-cyanamide
Cyanamide, [1-methyl-2-(phenylseleno)cyclohexyl]-, trans-
MLZOQQJOHSPKSE-UHFFFAOYSA-N
CIS-1-ACETYL-2-(1-(PHENYLSELENO)-1-(TRIMETHYLSILYL)-METHYL)-CYCLOPROPANE
trans-1-Acetyl-2-(1-(phenylseleno)-1-(trimethylsilyl)methyl)cyclopropane
Bicyclo[3.1.1]heptane-2-carboxaldehyde, 2-(phenylseleno)-
| Title | Journal or Book | Year |
|---|---|---|
| The Carbonyl Group as Homoconjugated Electron‐Releasing Substituent. Regioselective electrophilic additions at bicyclo[2.2.1]hept‐5‐en‐2‐one, bicyclo[2.2.2]oct‐5‐en‐2‐one, and derivatives | Helvetica Chimica Acta | 1989 |
| Factors influencing the nature of seleniranium ions in selenenyl chloride additions to alkenes: the use of methanol as solvent | Canadian Journal of Chemistry | 1980 |