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| | Methyl 5-amino-1H-1,2,4-triazole-3-carboxylate Basic information |
| Product Name: | Methyl 5-amino-1H-1,2,4-triazole-3-carboxylate | | Synonyms: | Methyl 3-aMino-1,2,4-triazole-5-carboxylate;Methyl 5-aMino-1,2,4-triazole-3-carboxylate;Methyl 5-AMino-1H-1,2,4-Triazole-3-Carboxylate Sulfate Salt;5-Amino-1H-[1,2,4]-triazole-3-carboxylic acid methyl ester 96%;1H-1,2,4-Triazole-3-carboxylicacid, 5-amino-, methyl ester;5-Amino-1H-[1, 2, 4]-triazole-3-carboxylic acid methyleester;2,4-triazole-3-carboxylicacid,5-amino-1h-methylester;5-AMINO-1H-1 2 4-TRIAZOLE-3-CARBOXYLIC | | CAS: | 3641-14-3 | | MF: | C4H6N4O2 | | MW: | 142.12 | | EINECS: | 222-869-7 | | Product Categories: | Building Blocks;Heterocyclic Building Blocks;Triazoles;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks | | Mol File: | 3641-14-3.mol |  |
| | Methyl 5-amino-1H-1,2,4-triazole-3-carboxylate Chemical Properties |
| Melting point | 218-222 °C (lit.) | | Boiling point | 379.0±25.0 °C(Predicted) | | density | 1.505±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | pka | 8.92±0.40(Predicted) | | form | Crystalline Powder | | color | White | | InChI | InChI=1S/C4H6N4O2/c1-10-3(9)2-6-4(5)8-7-2/h1H3,(H3,5,6,7,8) | | InChIKey | MGRNUMFYRVKLEO-UHFFFAOYSA-N | | SMILES | N1C(N)=NC(C(OC)=O)=N1 | | CAS DataBase Reference | 3641-14-3(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 43 | | Safety Statements | 36/37 | | WGK Germany | 3 | | HazardClass | IRRITANT | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Skin Sens. 1 |
| | Methyl 5-amino-1H-1,2,4-triazole-3-carboxylate Usage And Synthesis |
| Synthesis | To a solution of 5-amino-1H-1,2,4-triazole-3-carboxylic acid (3.9 g, 30.45 mmol) in methanol (100 mL) was slowly added thionyl chloride (SOCl2, 12 g, 100.84 mmol). The reaction mixture was stirred at 70 °C for 48 hours. Upon completion of the reaction, the mixture was concentrated under reduced pressure to remove the solvent. The residue was dissolved in water (100 mL) and the pH was adjusted with saturated sodium bicarbonate (NaHCO3) solution to 8. Subsequently, the aqueous phase was extracted with dichloromethane (3 x 50 mL). The organic layers were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford methyl 5-amino-1H-1,2,4-triazole-3-carboxylate as a white solid (800 mg, 65% yield). The product was confirmed by LC/MS (ES, m/z): [M + H]+ 143.0. 1H NMR (300 MHz, DMSO-d6): δ 3.85 (s, 3H). | | References | [1] Chemical and Pharmaceutical Bulletin, 2004, vol. 52, # 2, p. 192 - 198
[2] Russian Journal of Applied Chemistry, 2006, vol. 79, # 5, p. 783 - 786
[3] Patent: WO2014/66743, 2014, A1. Location in patent: Paragraph 0146 |
| | Methyl 5-amino-1H-1,2,4-triazole-3-carboxylate Preparation Products And Raw materials |
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