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| Names | |
|---|---|
| Preferred IUPAC name
 1,6-Dibromo-1,6-dideoxy-D-mannitol  | |
| Systematic IUPAC name
 1,6-Dibromohexane-2,3,4,5-tetrol[1]  | |
| Identifiers | |
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3D model (JSmol)  | 
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.006.979 | 
| EC Number | 
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| KEGG | |
| MeSH | Mitobronitol | 
PubChem CID  | 
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| RTECS number | 
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| UNII | |
CompTox Dashboard (EPA)  | 
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| Properties | |
| C6H12Br2O4 | |
| Molar mass | 307.966 g·mol−1 | 
| Appearance | Colourless crystals | 
| log P | −0.226 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol | 
| Acidity (pKa) | 12.609 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol | 
| Basicity (pKb) | 1.388 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol | 
| Pharmacology | |
| L01AX01 (WHO) | |
| Related compounds | |
Related compounds  | 
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
Mitobronitol (1,6-dibromo-1,6-dideoxy-D-mannitol) is a brominated analog of mannitol. It is an anticancer drug that is also classified as an alkylating agent.[2]
References
- ↑ "Mitolactol - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 25 March 2005. Identification. Retrieved 22 June 2012.
 - ↑ Mitobronitol, The Centre for Cancer Education
 
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