- 4-Iododibenzothiophene
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- $1.10 / 1g
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2025-11-18
- CAS:132034-89-0
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons
- 4-Iododibenzothiophene
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- $3.00 / 1KG
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2019-08-27
- CAS:132034-89-0
- Min. Order: 3KG
- Purity: 98%
- Supply Ability: 1kg,5kg,100kg
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| | 4-Iododibenzothiophene Basic information |
| Product Name: | 4-Iododibenzothiophene | | Synonyms: | 4-Iododibenzothiophene;4-Iododibenzo[b,d]thiophene;4-Iododibenzothiophene >Dibenzothiophene, 4-iodo-;4-Iododibenzothiophene ISO 9001:2015 REACH;6-iodo-8-thiatricyclo[7.4.0.02,?]trideca-1(9),2(7),3,5,10,12-hexaene;4-Iododibenzothiophen | | CAS: | 132034-89-0 | | MF: | C12H7IS | | MW: | 310.15 | | EINECS: | | | Product Categories: | | | Mol File: | 132034-89-0.mol |  |
| | 4-Iododibenzothiophene Chemical Properties |
| Melting point | 100.0 to 104.0 °C | | Boiling point | 408.2±18.0 °C(Predicted) | | density | 1.832±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | powder to crystal | | color | White to Orange to Green |
| | 4-Iododibenzothiophene Usage And Synthesis |
| Chemical Properties | off-white powder | | Synthesis | General procedure for the synthesis of 4-iododibenzothiophene from dibenzothiophene: To a stirred, cooled-to-0 °C solution of 2,2,6,6-tetramethylpiperidine (0.25 mL, 1.5 mmol) in tetrahydrofuran (THF, 2-3 mL) was sequentially added a hexane solution (1.5 mmol) of 1.6 M butyl lithium (BuLi) for 5 min followed by ZnCl2- TMEDA (0.13 g, 0.50 mmol). The reaction mixture was continued to be stirred at 0 °C for 15 min, followed by the addition of dibenzothiophene (1a, 0.20 g, 1.0 mmol). After 2 h of reaction at this temperature, a THF (4 mL) solution of iodine (I2, 0.38 g, 1.5 mmol) was added. The mixture was stirred overnight and then saturated aqueous sodium bicarbonate (NaHCO3) and sodium thiosulfate (Na2S2O3, 4 mL) solutions were added sequentially. The mixture was extracted with ethyl acetate (EtOAc, 3 x 20 mL), the organic layers were combined, dried with magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. Finally, the target product 4-iododibenzothiophene was purified by silica gel column chromatography (eluent: heptane/dichloromethane (CH2Cl2) gradient from 100:0 to 80:20). | | References | [1] Synthesis (Germany), 2017, vol. 49, # 19, p. 4500 - 4516 [2] Patent: KR2015/144121, 2015, A. Location in patent: Paragraph 0299-0301 [3] Patent: KR2016/26661, 2016, A. Location in patent: Paragraph 0679-0685 [4] Patent: KR101527181, 2015, B1. Location in patent: Paragraph 0111; 0112; 0113 [5] Journal of the American Chemical Society, 1945, vol. 67, p. 1479 |
| | 4-Iododibenzothiophene Preparation Products And Raw materials |
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