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TETRAIODOPHTHALIC ANHYDRIDE
TETRAIODOPHTHALIC ANHYDRIDE
- CAS No.632-80-4
- Chemical Name:TETRAIODOPHTHALIC ANHYDRIDE
- CBNumber:CB6193948
- Molecular Formula:C8I4O3
- Formula Weight:651.7
- MOL File:632-80-4.mol
TETRAIODOPHTHALIC ANHYDRIDE Property
- Melting point 327.5°C
- Boiling point 584.2±50.0 °C(Predicted)
- Density 3.1538 (estimate)
- EPA Substance Registry System 1,3-Isobenzofurandione, 4,5,6,7-tetraiodo- (632-80-4)
Safety
- HazardClass :IRRITANT
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H302
- Precautionary statements P280-P305+P351+P338
TETRAIODOPHTHALIC ANHYDRIDE Chemical Properties,Usage,Production
-
Preparation
CAUTION: This reaction should be carried out in a well-ventilated hood. <br/>To a flask equipped with a mechanical stirrer and an air condenser topped with a tube leading to a gas trap is added 74.0 gm (0.5 mole) of phthalic anhydride, 162 gm (0.638 mole) of iodine, and 300 ml of 60% fuming sulfuric acid (1.84 moles). The flask is gently heated to 45-50°C, at which point the reaction commences. If the reaction becomes too vigorous it may be necessary to use a ice bath to lower the temperature to 40-50°C. The reaction mixture is eventually (4 hr) heated up to 65°C until all visible reaction has ceased. The reaction mixture is cooled to 10-20°C and an additional 81.0 gm (0.318 mole) of iodine is added and the reaction again slowly heated up to 65°C (1?hr) and again when the reaction ceases it is cooled. Another 27.0 gm (0.107 mole) of iodine is added and the reaction is again heated up to 65°C (1 hr). The flask is heated with an oil bath to a bath temperature of 175-180°C, at which point the sulfur trioxide and iodine fumes evolve. After about 2 hr, when the gaseous evolution ceases, the flask is cooled to about 60°C and the mxiture then poured into a beaker of water. The contents are allowed to stand overnight at room temperature, filtered, washed with two 50-ml portions of cone, sulfuric acid and then with three 100 ml portions of water. The light yellow crystalline product is put into a beaker containing 1 liter of water and 10 gm of sodium bisulfite in order to remove the last traces of free iodine. The aqueous solution is decanted, the product washed five times with ? liter of water, washed twice with 100 ml of acetone and then dried at 60°C to afford 260-268 gm (80-82%), m.p. 327-328°C.
TETRAIODOPHTHALIC ANHYDRIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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632-80-4, TETRAIODOPHTHALIC ANHYDRIDERelated Search:
- 2-Iodobenzoic acid Methyl 2-iodobenzoate TETRAIODOPHTHALIC ANHYDRIDE 3,4,5-Triiodobenzyl alcohol Methyl 4-iodobenzoate 4-Iodobenzyl alcohol 1,2-Diiodobenzene 2,3,5-Triiodobenzoic acid 3,4-Diiodobenzoic acid 1-Iodo-2,3-dimethylbenzene 3-Iodobenzoic acid 3,4,5-Triiodobenzoic acid Methyl 3-iodobenzoate 3,5-Diiodobenzoic acid 3-Iodo-2-methylbenzoic acid 5-Iodo-2-methylbenzoic acid 4-Iodobenzoic acid 1,4-Diiodobenzene
- 合成材料中间体
- C8I4O3
- I4C6CO2O
- 4,5,6,7-TETRAIODOISOBENZOFURAN-1,4-DIONE
- 四碘苯酐
- 四碘邻苯二甲酸酐
- 四碘酞[酸]酐
- 632-80-4
- 3,4,5,6-Tetraiodophthalic anhydride
- TETRAIODOPHTHALIC ANHYDRIDE
- Phthalicanhydride,tetraiodo-
- 4,5,6,7-tetraiodo-3-isobenzofurandione
- 1,3-Isobenzofurandione,4,5,6,7-tetraiodo-
- 4,5,6,7-tetraiodo-1,3-Isobenzofurandione
- 4,5,6,7-tetraiodoisobenzofuran-1,3-quinone
- 4,5,6,7-tetraiodo-2-benzofuran-1,3-dione
- 4,5,6,7-tetraiodoisobenzofuran-1,3-dione