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Sigma-Aldrich |
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| | 4-(Ethoxycarbonyl)phenylzinc iodide Basic information |
| | 4-(Ethoxycarbonyl)phenylzinc iodide Chemical Properties |
| density | 1.018 g/mL at 25 °C | | Fp | 1 °F | | storage temp. | 2-8°C | | Water Solubility | Reacts with water. | | Sensitive | Air Sensitive | | InChI | 1S/C9H9O2.HI.Zn/c1-2-11-9(10)8-6-4-3-5-7-8;;/h4-7H,2H2,1H3;1H;/q;;+1/p-1 | | InChIKey | QKMCGFIQAJUQIL-UHFFFAOYSA-M | | SMILES | CCOC(=O)c1ccc([Zn]I)cc1 | | CAS DataBase Reference | 131379-16-3 |
| Hazard Codes | F,Xn | | Risk Statements | 14-19-22-36/38-40-36/37-11 | | Safety Statements | 16-26-33-36-36/37 | | RIDADR | UN 2056 3/PG 2 | | WGK Germany | 1 | | HazardClass | 4.3 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Acute Tox. 4 Oral Carc. 2 Eye Irrit. 2 Flam. Liq. 2 STOT SE 3 |
| | 4-(Ethoxycarbonyl)phenylzinc iodide Usage And Synthesis |
| Uses | 4-(Ethoxycarbonyl)phenylzinc iodide is used as pharmaceutical intermediates. | | Uses | 4-(Ethoxycarbonyl)phenylzinc iodide can be used as:
- A substrate in the transition metal-catalyzed cross-coupling reactions with unsaturated thioethers and thiomethyl-substituted N-heterocycles.
- A starting material in the synthesis of indazole derived glucagon receptor antagonists.
- A substrate in the Pd-catalyzed synthesis of 5-aryl-2-furaldehydes by reacting with 5-bromo-2-furaldehyde.
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| | 4-(Ethoxycarbonyl)phenylzinc iodide Preparation Products And Raw materials |
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