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| Ethyl 4-iodobenzoate Basic information |
| Ethyl 4-iodobenzoate Chemical Properties |
| Melting point | 267 °C | | Boiling point | 281-283 °C | | density | 1.641 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.5880(lit.) | | Fp | >230 °F | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform, Dichloromethane, Ethyl Acetate, Hexane | | form | Liquid | | Specific Gravity | 1.66 | | color | Clear colorless to yellow | | Water Solubility | insoluble | | Sensitive | Light Sensitive | | BRN | 2208568 | | CAS DataBase Reference | 51934-41-9(CAS DataBase Reference) | | NIST Chemistry Reference | Ethyl 4-iodobenzoate(51934-41-9) |
| Hazard Codes | N,Xi,C | | Risk Statements | 51/53-36/37/38 | | Safety Statements | 61-24/25 | | RIDADR | UN 3082 9/PG 3 | | WGK Germany | 3 | | F | 8 | | Hazard Note | Irritant | | HazardClass | IRRITANT, LIGHT SENSITIVE | | HS Code | 29163990 |
| Ethyl 4-iodobenzoate Usage And Synthesis |
| Chemical Properties | Light Yellow Oil | | Uses | Ethyl 4-iodobenzoate can be used in the synthesis of biphenyl derivatives via Negishi cross coupling with the intermediates of the type ArMg(tmp)·2LiCl (tmp = trimethylolpropane). It can also be used as a starting material in the synthesis of p-carbomethoxyphenylmagnesium bromide, a polyfunctional organometallic reagent that can be used as building block in the synthesis of complex target molecules. |
| Ethyl 4-iodobenzoate Preparation Products And Raw materials |
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