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| | N-(2-Aminoethyl)morpholine-4-carboxamide oxalate Basic information |
| Product Name: | N-(2-Aminoethyl)morpholine-4-carboxamide oxalate | | Synonyms: | N-(2-AMinoethyl)-4-MorpholinecarboxaMide ethanedio;N-(2-AMinoethyl)-4-MorpholinecarboxaMide;N-(2-aMinoethyl)-4-MorpholinecarboxaMide oxalate;N-(2-AMinoethyl)Morpholine-4-carboxaMide oxalate;Landiolol HCl
PI-3;N-(2-Aminoethyl)-4-Morpholinecarboxamide Ethanedioate,>98%;N-AMCO;N-(2-Aminoethyl)-4-morpholinecarboxamide ethanedioate ISO 9001：2015 REACH | | CAS: | 154467-16-0 | | MF: | C9H17N3O6 | | MW: | 263.25 | | EINECS: | 1308068-626-2 | | Product Categories: | | | Mol File: | 154467-16-0.mol |  |
| | N-(2-Aminoethyl)morpholine-4-carboxamide oxalate Chemical Properties |
| storage temp. | Inert atmosphere,Room Temperature | | Appearance | White to off-white Solid | | InChI | InChI=1S/C7H15N3O2.C2H2O4/c8-1-2-9-7(11)10-3-5-12-6-4-10;3-1(4)2(5)6/h1-6,8H2,(H,9,11);(H,3,4)(H,5,6) | | InChIKey | FMVSRINQKOORMK-UHFFFAOYSA-N | | SMILES | C(=O)(O)C(=O)O.C(N1CCOCC1)(=O)NCCN |
| | N-(2-Aminoethyl)morpholine-4-carboxamide oxalate Usage And Synthesis |
| Chemical Properties | The molecular structure of N-(2-aminoethyl)-4-morpholinecarboxamide oxalate consists of an N-(2-aminoethyl)-4-morpholinecarboxamide part and an oxalate part. Among them, the N-(2-aminoethyl)-4-morpholinecarboxamide portion is biologically active and is capable of interacting with certain receptors in living organisms, while the oxalate portion has the ability to regulate charge and solubility. This unique molecular structure gives N-(2-aminoethyl)-4-morpholinecarboxamide oxalate many excellent properties. | | Uses | N-(2-Aminoethyl)morpholine-4-carboxamide oxalate is a fine chemical raw material mainly used as epoxy resin. It is also used in proteomics research and in the synthesis of other products such as ethers, phenylchloropropane, propionic acid, etc. It is more commonly found in many household cleaning products. | | Synthesis | The preparation of N-(2-aminoethyl)-4-morpholinecarboxamide oxalate typically involves two key steps: first, N-(2-aminoethyl)-4-morpholinecarboxamide is synthesized, and then it is reacted with oxalate to obtain the target product. |
| | N-(2-Aminoethyl)morpholine-4-carboxamide oxalate Preparation Products And Raw materials |
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