It is used mainly as a reference compound in stereochemistry studies, carbohydrate research, and pharmaceutical synthesis. Its unique chirality allows selective incorporation into chemical reactions and the study of enantiomer-specific biological effects. L(-)-Glucose is the enantiomer of naturally occurring D-glucose, meaning it is a mirror-image form of the common sugar.
L(-)-Glucose
| API Name | Bleomycin |
|---|---|
| CAS No | 921-60-8 |
| Molecular Formula | C6H12O6 |
| Molecular Weight | 180.16 g/mol |
| Synonyms | (3S,4R,5R,6S)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol |
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Frequently Asked Questions
It is used mainly as a reference compound in stereochemistry studies, carbohydrate research, and pharmaceutical synthesis. Its unique chirality allows selective incorporation into chemical reactions and the study of enantiomer-specific biological effects. L(-)-Glucose is the enantiomer of naturally occurring D-glucose, meaning it is a mirror-image form of the common sugar.
The CAS number of L(-)-Glucose is 921-60-8.
The molecular formula of L(-)-Glucose is C6H12O6.
The listed molecular weight of L(-)-Glucose is 180.16 g/mol.
L(-)-Glucose is listed as being used in connection with the following API: Bleomycin.
The listed synonym or IUPAC name for L(-)-Glucose is (3S,4R,5R,6S)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol.