化工社化工社 化学情報印刷レポート · 研究参考用
1-フルオロ-2-ヨードエタン
1-フルオロ-2-ヨードエタン · 1-フルオロ-2-ヨードエタン, CONTAINS UP TO 1% COPPER POWDER AS STABILIZER · 1-fluor-2-jodethan · 2-fluoroethyliodide · 1-IODO-2-FLUOROETHANE · 2-FLUORO-1-IODOETHANE · 1-fluoro-2-iodo-ethan · 1-FLUORO-2-IODOETHANE

識別子と物理属性
| CAS No. | 762-51-6 |
|---|---|
| 分子式 | C2H4FI |
| 平均分子量 | 173.96 g/mol |
| 単同位体質量 | 173.93417635 g/mol |
| SMILES | FCCI |
| InChIKey | LVYJIIRJQDEGBR-UHFFFAOYSA-N |
| PubChem CID | 69804 |
| EC No. | 691-351-4 |
| DTXSID | DTXSID80227056 |
| 現地名 | 1-フルオロ-2-ヨードエタン |
化学・物理的性質
| XLogP | 1.7 |
|---|---|
| 極性表面積 | 0 |
| 水素結合供与体数 | 0 |
| 水素結合受容体数 | 1 |
| 回転可能結合数 | 1 |
| 重原子数 | 4 |
| 形式電荷 | 0 |
| 複雑度 | 10 |
| SpringerMaterials Properties | Coriolis coupling |
| 沸点 | 98-102°C |
| 密度 | 1.9842 (estimate) |
| 貯蔵条件 | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
| 外観・状態 | clear liquid |
| 色 | Colorless to Light yellow |
| InChI | InChI=1S/C2H4FI/c3-1-2-4/h1-2H2 |
| InChIKey | LVYJIIRJQDEGBR-UHFFFAOYSA-N |
| SMILES | C(F)CI |
化学的特性
Colorless liquid
安全性と法規制
| GHS 分類 | DangerH225 (50%): Highly Flammable liquid and vapor [Danger Flammable liquids]P210, P233, P240, P241, P242, P243, P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 6 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
|---|---|
| Hazard Classes and Categories | Flam. Liq. 2 (50%) |
| 税関コード | 29033990 |
| 危険文句(R) | 20/21/22 |
| 消防法 | 危-4-1-II |
| 危険表示 | T |
| hazard_note | Toxic |
| 安全措置(S) | 23-36/37/39-24/25 |
| 危険等級 | KEEP COLD, TOXIC |
用途
使用
1-Fluoro-2-iodoethane is used as a reagent in organic synthesis of several compounds including that of fluorinated U-50488 analogs for PET studies of kappa opioid receptors. It is also used in the synthesis of MK-3168, an imidazole analog which acts as a PET tracer for the imaging of brain fatty acid amide hydrolase.