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| | (1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene Basic information |
| Product Name: | (1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene | | Synonyms: | (1S,4S,8S) Carreira DOLEFIN Ligand, (1S,4S,8S)-5-Benzyl-2-isobutyl-8-methoxy-1,8-dimethyl-2-bicyclo[2.2.2]octa-2,5-diene;(1S,4S,8S)-5-Benzyl-2-isobutyl-8-methoxy-1,8-dimethylbicyclo[2.2.2]octa-2,5-diene
;(1s,4s,8s)-5-benzyl-2-isobutyl-8-methoxy-1,8-dimethyl-2-bicyclo[2.2.2]octa-2,5-diene;Bicyclo[2.2.2]octa-2,5-diene, 8-methoxy-1,8-dimethyl-2-(2-methylpropyl)-5-(phenylmethyl)-, (1S,4S,8S)-;(1S,4S,8S)-5-Benzyl-2-isobutyl-8-methoxy-1,8-dimethylbicyclo[2.2.2]octa-2,5-diene;(1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene | | CAS: | 862499-50-1 | | MF: | C22H30O | | MW: | 310.47 | | EINECS: | | | Product Categories: | | | Mol File: | 862499-50-1.mol | ![(1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene Structure](CAS/GIF/862499-50-1.gif) |
| | (1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene Chemical Properties |
| Boiling point | 392.1±42.0 °C(Predicted) | | density | 1.00±0.1 g/cm3(Predicted) | | refractive index | n20/D1.522 | | form | liquid | | Optical Rotation | [α]/D 84±5°, c = 0.5 in chloroform | | InChI | 1S/C22H30O/c1-16(2)11-19-13-20-18(12-17-9-7-6-8-10-17)14-21(19,3)15-22(20,4)23-5/h6-10,13-14,16,20H,11-12,15H2,1-5H3/t20-,21+,22-/m0/s1 | | InChIKey | ACWLDJOHMGJACE-BDTNDASRSA-N | | SMILES | CO[C@@]1(C)C[C@@]2(C)C=C(Cc3ccccc3)[C@@H]1C=C2CC(C)C |
| WGK Germany | 3 | | Storage Class | 10 - Combustible liquids |
| | (1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene Usage And Synthesis |
| Uses | Carreira DOLEFIN Ligands | | General Description | (1S,4S,8S)-5-Benzyl-2-isobutyl-8-methoxy-1,8-dimethylbicyclo[2.2.2]octa-2,5-diene, an enantiopure diene ligand developed by Carreira, is most commonly used in asymmetric catalysis. It is generally prepared from commercially available (R)-carvone. | | reaction suitability | reaction type: click chemistry |
| | (1S,4S,8S)-5-Benzyl-8-methoxy-1,8-dimethyl-2-(2'-methylpropyl)-bicyclo [2.2.2]octa-2,5-diene Preparation Products And Raw materials |
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