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| Formula | C6H8O6 |
| Net Charge | 0 |
| Average Mass | 176.124 |
| Monoisotopic Mass | 176.03209 |
| SMILES | [H][C@@]1([C@H](O)CO)OC(=O)C(O)=C1O |
| InChI | InChI=1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,5+/m1/s1 |
| InChIKey | CIWBSHSKHKDKBQ-MVHIGOERSA-N |
| Roles Classification |
|---|
| Chemical Role: | Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Brønsted base). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| D-ascorbic acid (CHEBI:51384) is a ascorbic acid (CHEBI:22652) |
| D-ascorbic acid (CHEBI:51384) is enantiomer of L-ascorbic acid (CHEBI:29073) |
| Incoming Relation(s) |
| L-ascorbic acid (CHEBI:29073) is enantiomer of D-ascorbic acid (CHEBI:51384) |
| IUPAC Names |
|---|
| (5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyfuran-2(5H)-one |
| D-threo-hex-2-enono-1,4-lactone |
| Synonyms | Source |
|---|---|
| D-lyxoascorbic acid | ChEBI |
| D-xyloascorbic acid | ChEBI |
| D-threo-hex-2-enoic acid γ-lactone | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Beilstein:84273 | Beilstein |
| CAS:10504-35-5 | ChemIDplus |