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| 2-Amino-4,6-dimethoxypyrimidine Basic information |
Product Name: | 2-Amino-4,6-dimethoxypyrimidine | Synonyms: | 4,6-Dimethoxypyrimidin-2-amine;2-Amino-4,6-dimethoxypyrimidine ,99%;2-Amino-4,6-dimethox;2-Amino-4,6-dimethoxypyrimidine ,97%;4,6-Dimethoxy-2-aminopyrimidine;4,6-Dimethoxy-2-pyrimidinylamine;6-diMethoxypyriMidine;4,6-dime | CAS: | 36315-01-2 | MF: | C6H9N3O2 | MW: | 155.15 | EINECS: | 252-969-6 | Product Categories: | Building Blocks;C6 to C8;Aromatics;Miscellaneous Reagents;Chemical Synthesis;Heterocyclic Building Blocks;Pyridines, Pyrimidines, Purines and Pteredines;Pyrimidine;Amines;Pyrimidines;Building Blocks;Heterocyclic Building Blocks;Heterocycle-Pyrimidine series;Aromatics, Miscellaneous Reagents | Mol File: | 36315-01-2.mol | |
| 2-Amino-4,6-dimethoxypyrimidine Chemical Properties |
Melting point | 94-96 °C (lit.) | Boiling point | 278.95°C (rough estimate) | density | 1.3092 (rough estimate) | refractive index | 1.6500 (estimate) | storage temp. | 2-8°C(protect from light) | solubility | Chloroform (Slightly), Methanol (Slightly) | form | Solid | pka | 4.02±0.10(Predicted) | color | White | InChI | InChI=1S/C6H9N3O2/c1-10-4-3-5(11-2)9-6(7)8-4/h3H,1-2H3,(H2,7,8,9) | InChIKey | LVFRCHIUUKWBLR-UHFFFAOYSA-N | SMILES | C1(N)=NC(OC)=CC(OC)=N1 | CAS DataBase Reference | 36315-01-2(CAS DataBase Reference) | EPA Substance Registry System | 2-Pyrimidinamine, 4,6-dimethoxy- (36315-01-2) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36-37/39 | WGK Germany | 3 | Hazard Note | Irritant | TSCA | Yes | HS Code | 29335995 |
| 2-Amino-4,6-dimethoxypyrimidine Usage And Synthesis |
Chemical Properties | Crystalline Powder | Uses | 2-Amino-4,6-dimethoxypyrimidine is a building block for various chemical synthesis. Attributes PIS available on request. Please contact us. Contact | Uses | 2-Amino-4,6-dimethoxypyrimidine is suitable for use in the preparation of cocrystal 2-amino-4,6-dimethoxypyrimidine-anthranilic acid (1/1). | General Description | 2-Amino-4,6-dimethoxypyrimidine is identified as degradation product of sulfosulphuron in agricultural soil by ESI LC-MS/MS analysis. It was isolated as metabolite during the biodegradation of bensulphuron-methyl by Penicillium pinophilum by liquid chromatography-mass spectrometry. The FTIR and FT-Raman spectra of 2-amino-4,6-dimethoxypyrimidine has been reported. Hydrogen bonding in the molecules of 2-amino-4,6-di-methoxy-pyrimidine has been investigated. |
| 2-Amino-4,6-dimethoxypyrimidine Preparation Products And Raw materials |
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