4-Iodopyrimidin-2-amine manufacturers
- 4-Iodopyrimidin-2-amine
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- $1.10 / 1g
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2025-11-18
- CAS:815610-16-3
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons Min
- 4-Iodopyrimidin-2-amine
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- $15.00 / 1KG
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2021-07-13
- CAS:815610-16-3
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
- 4-Iodopyrimidin-2-amine
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- $15.00 / 1KG
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2021-07-10
- CAS:815610-16-3
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| | 4-Iodopyrimidin-2-amine Basic information |
| | 4-Iodopyrimidin-2-amine Chemical Properties |
| Boiling point | 364.9±34.0 °C(Predicted) | | density | 2.204±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 3.27±0.10(Predicted) | | Appearance | Off-white to light brown Solid |
| | 4-Iodopyrimidin-2-amine Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of 2-amino-4-iodopyrimidine using 2-amino-4-chloropyrimidine as starting material was as follows: 2-amino-4-chloropyrimidine (13.0 g, 100 mmol) was slowly added to 57 wt% aqueous hydriodic acid solution (115 mL, 1.00 mol) at 0 °C. The reaction mixture was stirred continuously for 3 hours at room temperature. Subsequently, the mixture was cooled to 0 °C and the resulting precipitate was removed by filtration. The filter cake was transferred to a pre-cooled aqueous 5 N Na2CO3 solution (200 mL). The aqueous phase was extracted using ethyl acetate (3 × 500 mL), and the combined organic phases were concentrated under reduced pressure to afford 2-amino-4-iodopyrimidine (21.1 g, 95.0 mmol, 95% yield) as a white solid. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 7.78 (d, J = 5.0 Hz, 1H), 7.02 (br.s, 2H), 7.00 (d, J = 5.0 Hz, 1H). The mass spectrum (ESI, cation mode) showed m/z: 222.1 ([M + H]+). | | References | [1] European Journal of Medicinal Chemistry, 2014, vol. 80, p. 364 - 382
[2] Organic Letters, 2014, vol. 16, # 3, p. 708 - 711 |
| | 4-Iodopyrimidin-2-amine Preparation Products And Raw materials |
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