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| | (1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane Basic information |
| Product Name: | (1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane | | Synonyms: | 2,2'-[(1S,2S,4S,5S)-BICYCLO[2.2.1]HEPTANE-2,5-DIYLBIS(NITRILOMETHYL)]BIS(4,6-DI-TERT-BUTYLPHENOL);2,2'-[(1S,2S,4S,5S)-Bicyclo[2.2.1]heptane-2,5-diylbis(nitrilomethylidyne)]bis[4,6-bis(1,1-dimethylethyl)phenol];2'-[(1S;(1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane>Phenol, 2,2'-[(1S,2S,4S,5S)-bicyclo[2.2.1]heptane-2,5-diylbis(nitrilomethylidyne)]bis[4,6-bis(1,1-dimethylethyl)- (9CI);6,6'-((1E,1'E)-((1S,2S,4S,5S)-Bicyclo[2.2.1]heptane-2,5-diylbis(azanylylidene))bis(methanylylidene))bis(2,4-di-tert-butylphenol);(1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane | | CAS: | 539834-16-7 | | MF: | C37H54N2O2 | | MW: | 558.84 | | EINECS: | | | Product Categories: | Asymmetric Synthesis;Synthetic Organic Chemistry | | Mol File: | 539834-16-7.mol | ![(1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane Structure](CAS/GIF/539834-16-7.gif) |
| | (1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane Chemical Properties |
| Melting point | 254 °C | | Boiling point | 625.1±55.0 °C(Predicted) | | density | 1.05±0.1 g/cm3(Predicted) | | pka | 13.33±0.40(Predicted) | | form | powder to crystal | | color | Light yellow to Yellow to Orange |
| | (1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane Usage And Synthesis |
| Uses | (1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane is a ligand used in the preparation of chromium-based catalysts for the asymmetric Nozaki-Hiyama-Kishi addition of aldehydes and allyl and vinyl halides. |
| | (1S,2S,4S,5S)-2,5-Bis(3,5-di-tert-butyl-2-hydroxybenzylideneamino)bicyclo[2.2.1]heptane Preparation Products And Raw materials |
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