≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
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 |
| Kanonisches Lächeln | CC(CC=C)O |
| IUPAC Name | (2S)-pent-4-en-2-ol |
| InChIKey | ZHZCYWWNFQUZOR-YFKPBYRVSA-N |
| INCHI | 1S/C5H10O/c1-3-4-5(2)6/h3,5-6H,1,4H2,2H3/t5-/m0/s1 |
| Isomere SMILES | C[C@@H](CC=C)O |
| PubChem CID | 6994332 |
| Molekulargewicht | 86.13 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Klasse | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Secondary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 I2608164 | Certificate of Analysis | Sep 21, 2026 | S467331 |
| H23031027 | Certificate of Analysis | May 13, 2026 | S467331 |
| H23021027 | Certificate of Analysis | Jul 17, 2023 | S467331 |
| H23031041 | Certificate of Analysis | Jul 17, 2023 | S467331 |
| H23031045 | Certificate of Analysis | Jul 17, 2023 | S467331 |
| F2309425 | Certificate of Analysis | May 08, 2023 | S467331 |
| F2309453 | Certificate of Analysis | May 08, 2023 | S467331 |
| Molekulargewicht | 86.130 g/mol |
|---|---|
| XLogP3 | 1.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 86.0732 Da |
| Monoisotopic Mass | 86.0732 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 41.200 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
