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Page 123
>> (2R,4S)-Rel-4-(Phosphonomethyl)-2-Piperidinecarboxylicacid
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(2R,4S)-Rel-4-(Phosphonomethyl)-2-Piperidinecarboxylicacid [110347-85-8]
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| Name |
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(2R,4S)-Rel-4-(Phosphonomethyl)-2-Piperidinecarboxylicacid |
| Synonyms |
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(2S,4R)-4-(Phosphonomethyl)-2-Piperidinecarboxylic Acid; (2S,4R)-4-(Phosphonomethyl)Pipecolinic Acid; Cgs 19755 |
| Molecular Formula |
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C7H14NO5P |
| Molecular Weight |
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223.17 |
| CAS Registry Number |
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110347-85-8 |
| SMILES |
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[C@@H]1(C[C@H](NCC1)C(O)=O)C[P](O)(O)=O |
| InChI |
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1S/C7H14NO5P/c9-7(10)6-3-5(1-2-8-6)4-14(11,12)13/h5-6,8H,1-4H2,(H,9,10)(H2,11,12,13)/t5-,6+/m1/s1 |
| InChIKey |
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LPMRCCNDNGONCD-RITPCOANSA-N |
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Properties
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Desity |
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1.44g/cm3 (Cal.) |
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Boiling point |
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508.595°C at 760 mmHg (Cal.) |
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Flash point |
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261.389°C (Cal.) |
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References
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Taichi Kano, Takeshi Kumano, Ryu Sakamoto and Keiji Maruoka. Catalytic asymmetric synthesis of cyclic amino acids and alkaloid derivatives: application to (+)-dihydropinidine and Selfotel synthesis, Chem. Sci., 2010, 1, 499.
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