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4-Iododibenzothiophene

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CAS:132034-89-0
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CAS:132034-89-0
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4-Iododibenzothiophene manufacturers

  • 4-Iododibenzothiophene
  • 4-Iododibenzothiophene pictures
  • $3.00 / 1KG
  • 2019-08-27
  • CAS:132034-89-0
  • Min. Order: 3KG
  • Purity: 98%
  • Supply Ability: 1kg,5kg,100kg
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 Structure
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
Safety Information
HS Code 2934.99.4400
MSDS Information
4-Iododibenzothiophene Usage And Synthesis
Chemical Propertiesoff-white powder
Synthesis
Dibenzothiophene

132-65-0

4-Iododibenzothiophene

132034-89-0

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
Raw materialsDibenzothiophene-->n-Butyllithium-->2,2,6,6-Tetramethylpiperidine-->Hexane-->iodine-->Tetrahydrofuran
Preparation Products12H- [1] benzothieno [2,3-a] carbazole
Tag:4-Iododibenzothiophene(132034-89-0) Related Product Information
Dibenzofuran

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