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| | 7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane Basic information |
| Product Name: | 7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane | | Synonyms: | 3-Benzyl-7-tert-butoxycarbonyl-3,7-diazabicyclo[3.3.1]nonane;tert-Butyl 7-benzyl-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate;1,1-Dimethylethyl 7-(phenylmethyl)-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate;3-Benzyl-7-Boc-3,7-diazabicyclo[3.3.1]nonane;7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane | | CAS: | 227940-71-8 | | MF: | C19H28N2O2 | | MW: | 316.44 | | EINECS: | | | Product Categories: | pharmacetical | | Mol File: | 227940-71-8.mol | ![7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane Structure](CAS/GIF/227940-71-8.gif) |
| | 7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane Chemical Properties |
| Melting point | 62-65℃ | | Boiling point | 409.1±38.0 °C(Predicted) | | density | 1.097 | | storage temp. | Sealed in dry,Room Temperature | | pka | 8.13±0.20(Predicted) | | Appearance | White to light yellow Solid |
| | 7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane Usage And Synthesis |
| Uses | tert-Butyl 7-Benzyl-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate is a reactant used in the preparation of chiral phosphoramidite ligands for enantioselective conjugate addition reactions. | | References | [1] Tetrahedron Letters, 2012, vol. 53, # 6, p. 623 - 626
[2] Physical Chemistry Chemical Physics, 2016, vol. 18, # 22, p. 15046 - 15053
[3] Journal of the American Chemical Society, 2008, vol. 130, # 17, p. 5654 - 5655
[4] Advanced Synthesis and Catalysis, 2008, vol. 350, # 13, p. 2001 - 2006
[5] Russian Chemical Bulletin, 2016, vol. 65, # 10, p. 2479 - 2484 |
| | 7-Benzyl-3-Boc-3,7-diazabicyclo[3.3.1]nonane Preparation Products And Raw materials |
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