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4,5-二氨基-6-氯嘧啶
6-氯-4,5-嘧啶二胺 · 6-氯嘧啶-4,5-二胺 · 6-氯-4,5-二氨基嘧啶 · 4,5-二氨基-6-氯嘧啶 · 4,5-二氨基-6-氯嘧啶 1G · 4-氨基-6-氯嘧啶-5-基-胺 · 4,5-二氨基-6-氯嘧啶,6-氯-4,5-二氨基嘧啶,6-氯-4,5-嘧啶二胺 · 6-Chloropyrimidine-4,5-diamine

标识与物理属性
| CAS No. | 4316-98-7 |
|---|---|
| 分子式 | C4H5ClN4 |
| 平均分子量 | 144.56 g/mol |
| 单同位素质量 | 144.02027384 g/mol |
| SMILES | Nc1ncnc(Cl)c1N |
| InChIKey | VNSFICAUILKARD-UHFFFAOYSA-N |
| PubChem CID | 78010 |
| EC No. | 224-341-1 |
| DTXSID | DTXSID8063410 |
| 中文名 | 4,5-二氨基-6-氯嘧啶 |
化学与物理性质
| XLogP | 0.1 |
|---|---|
| 极性表面积 | 77.8 |
| 氢键供体 | 2 |
| 氢键受体 | 4 |
| 可旋转键 | 0 |
| 重原子 | 9 |
| 形式电荷 | 0 |
| 复杂度 | 98.6 |
| 熔点 | 252 °C (decomp) |
| 沸点 | 336.7±37.0 °C(Predicted) |
| 密度 | 1.565 |
| 闪点 | 157℃ |
| 储存条件 | under inert gas (nitrogen or Argon) at 2–8 °C |
| 溶解性 | DMSO (Sparingly), Methanol (Slightly) |
| pKa(酸度系数) | 2.39±0.10(Predicted) |
| 形态 | powder to crystal |
| 颜色 | White to Amber to Dark green |
| 最大波长(λmax) | 305nm(lit.) |
| 稳定性 | Hygroscopic |
| InChI | InChI=1S/C4H5ClN4/c5-3-2(6)4(7)9-1-8-3/h1H,6H2,(H2,7,8,9) |
| InChIKey | VNSFICAUILKARD-UHFFFAOYSA-N |
| SMILES | C1=NC(Cl)=C(N)C(N)=N1 |
| CAS 数据库 | 4316-98-7 |
| EPA化学物质信息 | 4,5-Pyrimidinediamine, 6-chloro- (4316-98-7) |
安全与法规
| GHS 分类 | WarningH302 (95%): Harmful if swallowed [Warning Acute toxicity, oral]P261, P264, P264+P265, P270, P272, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P333+P317, P337+P317, P362+P364, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
|---|---|
| Hazard Classes and Categories | Acute Tox. 4 (95%) |
| TSCA 清单状态 | TSCA listed |
| 安全说明(S) | 26-36 |
| 海关编码 | 29335990 |
| 危险类别码(R) | 36/37/38 |
制备与合成方法
生产方法
步骤1:将4,6-二氯嘧啶-5-胺(1.64g,10mmol)悬浮于5mL浓盐酸中。将该悬浮液转移至密封管中,加入氨水溶液,于100℃下搅拌反应过夜。反应完成后,过滤收集固体产物,经真空干燥,得到目标化合物6-氯嘧啶-4,5-二胺,为黄色固体(1.2g,产率83%)。LC-MS分析显示:m/z 145([M+H]+)。参考文献:[1] Patent: WO2006/46023, 2006, A1. Location in patent: Page/Page column 115-116[2] Patent: WO2008/75110, 2008, A1. Location in patent: Page/Page column 116[3] Patent: WO2007/125315, 2007, A2. Location in patent: Page/Page column 115[4] Patent: WO2007/125325, 2007, A1. Location in patent: Page/Page column 92-93[5] Organic Process Research and Development, 2011, vol. 15, # 4, p. 841 - 854