Identification | Back Directory | [Name]
4-(ETHOXYCARBONYL)PHENYLZINC IODIDE | [CAS]
131379-16-3 | [Synonyms]
Ethyl 4-(iodozincio)benzoate 4-(ETHOXYCARBONYL)PHENYLZINC IODIDE 4-(Iodozincio)benzoic acid ethyl ester 4-(ethoxycarbonyl)phenylzinc iodide solution 4-(Ethoxycarbonyl)phenylzinc iodide solution 0.5 in THF 4-(Ethoxycarbonyl)phenylzinc iodide solution 0.5M in THF 4-(ETHOXYCARBONYL)PHENYLZINC IODIDE, 0.5 M SOLUTION IN TETRAHYDROFURAN 4-(Ethoxycarbonyl)phenylzinc iodide, Packaged under Argon in resealable ChemSeal? bottles | [Molecular Formula]
C9H9IO2Zn | [MDL Number]
MFCD00671982 | [MOL File]
131379-16-3.mol | [Molecular Weight]
341.46 |
Chemical Properties | Back Directory | [density ]
1.018 g/mL at 25 °C
| [Fp ]
1 °F
| [storage temp. ]
2-8°C | [Water Solubility ]
Reacts with water. | [Sensitive ]
Air Sensitive | [Exposure limits]
ACGIH: TWA 50 ppm; STEL 100 ppm (Skin) OSHA: TWA 200 ppm(590 mg/m3) NIOSH: IDLH 2000 ppm; TWA 200 ppm(590 mg/m3); STEL 250 ppm(735 mg/m3) | [CAS DataBase Reference]
131379-16-3 |
Hazard Information | Back Directory | [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.
| [Uses]
4-(Ethoxycarbonyl)phenylzinc iodide is used as pharmaceutical intermediates. |
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