3H-1,2-苯并二磺酚-3-酮
3H-1,2-苯并二磺酚-3-酮结构式
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常用名 | 3H-1,2-苯并二磺酚-3-酮 | 英文名 | 3H-1,2-BENZODITHIOL-3-ONE |
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| CAS号 | 1677-27-6 | 分子量 | 168.23600 | |
| 密度 | N/A | 沸点 | 337.6°C at 760 mmHg | |
| 分子式 | C7H4OS2 | 熔点 | 74-77 ℃(lit.) | |
| MSDS | 中文版 美版 | 闪点 | N/A |
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Use of 1,2,4-dithiazolidine-3,5-dione (DtsNH) and 3-ethoxy-1,2,4-dithiazoline-5-one (EDITH) for synthesis of phosphorothioate-containing oligodeoxyribonucleotides.
Nucleic Acids Res. 24(9) , 1602-7, (1996) Previous methods for the preparation of phosphorothioate-containing oligodeoxyribonucleotides rely on the reaction of phosphite triesters with sulfurizing reagents such as tetraethylthiuram disulfide (TETD) and 3H-1,2-benzodithiol-3-one 1,1-dioxide (Beaucage ... |
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Possible chemical mechanisms underlying the antitumor activity of S-deoxyleinamycin.
Bioorg. Med. Chem. Lett. 18 , 3076-80, (2008) Though less potent than the parent natural product leinamycin, S-deoxyleinamycin displays activity against human cancer cell lines that is comparable to many clinically used agents. The results reported here suggest that the 1,2-dithiolan-3-one heterocycle fo... |
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Novel syntheses of dithiosalicylide. Mitra K and Gates KS.
Tetrahedron Lett. 36(9) , 1391-94, (1995)
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Nucleoside H-phosphonates. 13. Studies on 3H-1, 2-benzodithiol-3-one derivatives as sulfurizing reagents for H-phosphonate and H-phosphonothioate diesters. Stawinski J and Thelin M.
J. Org. Chem. 56(17) , 5169-5175, (1991)
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