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Description
(S)-(+)-4-Penten-2-ol can be used:As an intermediate in one of the key synthetic steps for the preparation of undecenolide (−)-cladospolide C.To prepare a carboxamide derivative as a key intermediate for the preparation of (−)-iso-cladospolide B1.To prepareS-enantiomers of hydroxyeicosa tetraenoic acid named 19-HETE.To prepare an acryloyl ester derivative by reacting with acryloyl chloride, which is a key intermediate for the synthesis of parasorbic acid.
| CAS | 55563-79-6 |
|---|---|
| Synonymes | (S)-(+)-4-Penten-2-ol, 95% | (2S)-4-penten-2-ol | (2s)-4penten-2-ol | ZHZCYWWNFQUZOR-YFKPBYRVSA-N | (A+/-)-pent-4-en-2-ol | AKOS015840154 | (2S)-pent-4-en-2-ol | (S)-(+)-4-Penten-2-ol | 4-Penten-2-ol, (2S)- | EN300-211432 | MFCD03427200 | (S)-pent-4-en-2- |
| Spécifications et pureté | ≥95% |
| Conditions de stockage de stockage | Room temperature |
| Product Description | Description (S)-(+)-4-Penten-2-ol can be used:As an intermediate in one of the key synthetic steps for the preparation of undecenolide (−)-cladospolide C.To prepare a carboxamide derivative as a key intermediate for the preparation of (−)-iso-cladospolide B1.To prepareS-enantiomers of hydroxyeicosa tetraenoic acid named 19-HETE.To prepare an acryloyl ester derivative by reacting with acryloyl chloride, which is a key intermediate for the synthesis of parasorbic acid. |
| Pubchem Sid | 504764456 |
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504764456 |
| Numéro Mdl | MFCD03427200 |
| Numéro CE | 626-193-7 |
| PubChem CID | 6994332 |