l-Deoxyribose is an organic compound with formula C5H10O4. It is a synthetic monosaccharide, a stereoisomer (mirror image) of the natural compound d-deoxyribose.
Quick Facts Names, Identifiers ...
l-Deoxyribose
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Names |
IUPAC name
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Systematic IUPAC name
(3 R,4 S)-3,4,5-Trihydroxypentanal 2-Deoxy- l- erythro-pentose [2] |
Other names
2-Deoxy-l-ribose; l-2-Deoxyribose |
Identifiers |
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ChemSpider |
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ECHA InfoCard |
100.131.283 |
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InChI=1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1 N Key: ASJSAQIRZKANQN-UHNVWZDZSA-N N InChI=1/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1 Key: ASJSAQIRZKANQN-UHNVWZDZBB hemiacetal: InChI=1/C5H10O4/c6-2-4-3(7)1-5(8)9-4/h3-8H,1-2H2/t3-,4+,5?/m1/s1 Key: PDWIQYODPROSQH-OVEKKEMJBQ hemiacetal: InChI=1S/C5H10O4/c6-2-4-3(7)1-5(8)9-4/h3-8H,1-2H2/t3-,4+,5?/m1/s1 Key: PDWIQYODPROSQH-OVEKKEMJSA-N
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O=CC[C@@H](O)[C@@H](O)CO hemiacetal: OC[C@@H]1OC(O)C[C@H]1O
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Properties |
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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).
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Close
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]