| Weight | 289.375 g/mol |
|---|---|
| Formula | C8H19NO6S2 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
IMPROSULFAN (13425-98-4)
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- Antitumor activity of improsulfan by the fractionated dose schedule on rat ascites tumors. (Chemical & Pharmaceutical Bulletin, 1976)
- [Lethal effect of improsulfan tosylate on cultured mammalian cells (author's transl)]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1976)
- Increased lifespan by the sequential treatment with improsulfan and cyclophosphamide in rats bearing Yoshida ascites sarcoma. (Chemical & Pharmaceutical Bulletin, 1976)
- Antitumor effectiveness of improsulfan on nitrogen mustard-resistant yoshida sarcoma cells. (Chemical & Pharmaceutical Bulletin, 1977)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCS(=O)(=O)OCCCNCCCOS(=O)(=O)C
-
InChIKeyDBIGHPPNXATHOF-UHFFFAOYSA-N
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Safety
Alternate Names
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Synthesis
Reactant
+
3-chloropropyl methanesulfonate
(Alkylation of primary amines)
Methanesulfonyl chloride
+
Reactant
(O-sulfonylation)
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