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| | 2,4-Dinitroiodobenzene Basic information |
| Product Name: | 2,4-Dinitroiodobenzene | | Synonyms: | 6-IODO-1,3-DINITROBENZENE;1-IODO-2,4-DINITROBENZENE;2,4-DINITRO-1-IODOBENZENE;2,4-DINITROIODOBENZENE;Benzene, 1-iodo-2,4-dinitro-;AKOS 90747;2,4-Dinitroiodobenzene,98%;2,4-Dinitroiodobenzene > | | CAS: | 709-49-9 | | MF: | C6H3IN2O4 | | MW: | 294 | | EINECS: | 211-908-3 | | Product Categories: | API intermediates;Nitro Compounds;Nitrogen Compounds;Organic Building Blocks | | Mol File: | 709-49-9.mol |  |
| | 2,4-Dinitroiodobenzene Chemical Properties |
| Melting point | 86-88 °C(lit.) | | Boiling point | 351.8±32.0 °C(Predicted) | | density | 2.174±0.06 g/cm3(Predicted) | | form | powder to crystal | | color | Light yellow to Yellow to Orange | | Water Solubility | Insoluble in water. | | Sensitive | Light Sensitive | | BRN | 1113584 | | CAS DataBase Reference | 709-49-9(CAS DataBase Reference) | | NIST Chemistry Reference | 2,4-Dinitroiodobenzene(709-49-9) |
| Hazard Codes | Xn | | Risk Statements | 42/43 | | Safety Statements | 22-26-37 | | WGK Germany | 3 | | HS Code | 2904.20.4500 |
| | 2,4-Dinitroiodobenzene Usage And Synthesis |
| Uses | It is employed in the cloning and characterization of a biotic-stress-inducible glutathione transferase from Phaseolus vulgaris. | | Definition | ChEBI: Iodobenzene substituted at C-2 and -4 with nitro groups. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 23, p. 305, 1958 DOI: 10.1021/jo01096a608 | | Purification Methods | Crystallise it from EtOAc. [Beilstein 5 H 270.] |
| | 2,4-Dinitroiodobenzene Preparation Products And Raw materials |
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