3H-1,2-BENZODITHIOL-3-ONE
3H-1,2-BENZODITHIOL-3-ONE structure
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Common Name | 3H-1,2-BENZODITHIOL-3-ONE | ||
|---|---|---|---|---|
| CAS Number | 1677-27-6 | Molecular Weight | 168.23600 | |
| Density | N/A | Boiling Point | 337.6°C at 760 mmHg | |
| Molecular Formula | C7H4OS2 | Melting Point | 74-77 ℃(lit.) | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Name | 1,2-benzodithiol-3-one |
|---|---|
| Synonym | More Synonyms |
| Boiling Point | 337.6°C at 760 mmHg |
|---|---|
| Melting Point | 74-77 ℃(lit.) |
| Molecular Formula | C7H4OS2 |
| Molecular Weight | 168.23600 |
| Exact Mass | 167.97000 |
| PSA | 73.55000 |
| LogP | 2.32300 |
| Precursor 0 | |
|---|---|
| DownStream 10 | |
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CAS#:66304-00-5| HS Code | 2930909090 |
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| Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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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 ... |
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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 report... |
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Novel syntheses of dithiosalicylide. Mitra K and Gates KS.
Tetrahedron Lett. 36(9) , 1391-94, (1995)
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| 3H-1,2-Benzodithiol-3-one |
| EINECS 216-829-8 |
| MFCD00134412 |