| 
 | |||
| Names | |||
|---|---|---|---|
| IUPAC name 2-Deoxy-l-ribose [1]  | |||
| Systematic IUPAC name | |||
| Other names 2-Deoxy-l-ribose; l-2-Deoxyribose | |||
| Identifiers | |||
| 3D model (JSmol) | 
 | ||
| ChemSpider | |||
| ECHA InfoCard | 100.131.283 | ||
|  PubChem CID | |||
|  CompTox Dashboard (EPA) | |||
| 
 | |||
| 
 | |||
| Properties | |||
| C5H10O4 | |||
| Molar mass | 134.131 g·mol−1 | ||
| Appearance | White solid | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
l-Deoxyribose is an organic compound with formula C5H10O4. It is a synthetic monosaccharide, a stereoisomer (mirror image) of the natural compound d-deoxyribose.
l-Deoxyribose can be synthesized from d-galactose. [3] It has been used in chemical research, e.g. in the synthesis of mirror-image DNA. [4]