| Weight | 128.175 g/mol |
|---|---|
| Formula | C6H12N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
N-methylpyrrolidine-3-carboxamide (1007870-02-1)
N-methyl-3-pyrrolidinecarboxamide · 1007870-02-1
Suppliers
Most-cited Publications
- Practical Asymmetric Synthesis of (R)-(-)-Carnitine Catalyzed by (2R,4R)-4-(Dicyclohexylphosphino)-2-(di-3,5-xylylphosphinomethyl)-N-methyl-1-pyrrolidinecarboxamide-Rhodium Complex1 (Synlett, 1991)
- Disposition and metabolism of 3-(3-chlorophenoxy)-N-methylpyrrolidine [14C]-carboxamide in the rat, dog, and man. (Drug Metabolism and Disposition, 1976)
- Crystalline forms(2s)-n-5[amino(imino)methyl]-2-thienylmethyl-1-(2r)-2[(carboxymethyl) amino]-3,3-diphenylpropanoyl-2-pyrrolidinecarboxamide nh2o (2003)
- ChemInform Abstract: Asymmetric Reactions Catalyzed by Chiral Metal Complexes. Part 43. Practical Asymmetric Synthesis of (R)()Carnitine (I) Catalyzed by ( 2R,4R)4(Dicyclohexylphosphino)2(di3,5xylylphosphinomethyl)N methyl1pyrrolidinecarboxamideRhodium Complex. (ChemInform, 2010)
- Crystalline forms of (S)-1-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyrrolo[1,2-f][1,2,4]triazin-2-yl)-N-(6-fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide (2011)
Alternate Names
- N-methyl-3-pyrrolidinecarboxamide
- 1007870-02-1
-
SMILESCNC(=O)C1CCNC1
-
InChIKeyBVOWXWSHDIGNRE-UHFFFAOYSA-N
Estimated Properties
| Boiling Point | 235.03 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 296.56 C | EPI Suite |
| Density | 1.02 g/cm3 | EPA T.E.S.T. |
| Flash Point | 147.72 C | EPA T.E.S.T. |
| Melting Point | 98.09 C | EPI Suite |
| Water Solubility | 34214.2 mg/L | EPA T.E.S.T. |
| Water Solubility | 1e+06 mg/L | EPI Suite |
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