thianthrene 5-oxide

thianthrene 5-oxide Suppliers list
Company Name: Henan Alfa Chemical Co., Ltd
Tel: +8618339805032
Email: alfa4@alfachem.cn
Products Intro: CAS:2362-50-7
Purity:97%+ Package:5g; 25g; 100g; 500g; 1kg; 25kg
Company Name: Aladdin Scientific
Tel: +1-833-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:Thianthrene 5-oxide
CAS:2362-50-7
Purity:97% Package:$40.9/100mg;$82.9/250mg;$127.9/1g;$491.9/5g;Bulk package Remarks:97%
Company Name: Bide Pharmatech Ltd.  
Tel: 400-1647117 15221909166
Email: product02@bidepharm.com
Products Intro: Product Name:Thianthrene 5-oxide
CAS:2362-50-7
Purity:97% Package:100mg;250mg;1g;5g;
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Tel: 025-66113011 18112977050
Email: cb6@aikonchem.com
Products Intro: CAS:2362-50-7
Purity:95+% Package:1g;5g;10g
Company Name: MQ (shanghai) Pharmaceuticals Co., Ltd.  
Tel: 13761635123
Email: 1014988033@qq.com
Products Intro: Product Name:Thianthrene 5-oxide
CAS:2362-50-7
Purity:>95% Package:1G,5G
thianthrene 5-oxide Basic information
Product Name:thianthrene 5-oxide
Synonyms:thianthrene 5-oxide;Thianthrene 10-oxide;Benzothianthrene Oxide
CAS:2362-50-7
MF:C12H8OS2
MW:232.32
EINECS:
Product Categories:
Mol File:2362-50-7.mol
thianthrene 5-oxide Structure
thianthrene 5-oxide Chemical Properties
Melting point 143-143.5 °C
Boiling point 423.2±15.0 °C(Predicted)
density 1.49±0.1 g/cm3(Predicted)
storage temp. 2-8°C
Safety Information
MSDS Information
thianthrene 5-oxide Usage And Synthesis
UsesThianthrene S-oxide is a sulfoxide-based thianthrene reagent for late-stage C-H functionalization. Developed by the Ritter Lab, C-H functionalization by thianthrenation proceeds with >99% selectivity and furnishes functionalized arenes serving as synthetic linchpins for further participation in diverse transformations. Nonfluorinated thianthrene S-oxide is best used for all arenes more electron-rich than anisole. For other arenes, the fluorinated TFT S-oxide (903981) was demonstrated as the thanthrenation reagent.
Synthesis Reference(s)Journal of the American Chemical Society, 78, p. 2163, 1956 DOI: 10.1021/ja01591a037
Synthetic Communications, 22, p. 1799, 1992 DOI: 10.1080/00397919208020500
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