4-Penten-1-ol
pent-4-en-1-ol
Résumé du produit
Aperçu rapide
- Famille de produits
- Click Chemistry & Bioconjugation Reagents
- Nom chimique
- pent-4-en-1-ol
- FM
- C5H10O
- PM
- 86.13
- Pureté
- 99.58% (GC)
4-Penten-1-ol is a terminal alkene alcohol also indexed as pent-4-en-1-ol, 4-pentenol, 4-pentenyl alcohol, and 5-hydroxy-1-pentene.
CH63015 is listed with CAS 821-09-0, molecular formula C5H10O, and molecular weight 86.13. Research literature links 4-Penten-1-ol with thiol-ene dendrimer-materials research, Ru-catalyzed cross-metathesis, and halocyclization mechanism studies of terminal alkenyl alcohols.
Identité et spécifications
| Catalog No. | CH63015 |
| CAS No. | 821-09-0 |
| Chemical Name | pent-4-en-1-ol |
| Molecular Formula | C5H10O |
| Molecular Weight | 86.13 |
| PubChem CID | 13181 |
| InChIKey | LQAVWYMTUMSFBE-UHFFFAOYSA-N |
| Purity | 99.58% (GC) |
Conditions de stockage
Room temperature; cool and dark place below 15 C
Caractéristiques techniques
- Building-block class
- Terminal-alkene alcohol
- Reactive handle
- Terminal alkene
- Complementary handle
- Primary alcohol
- Supported chemistry
- Thiol-ene modification
- Packaging
- 25 mL; 250 mL; Custom packaging on request
- Water content
- Water (KF) 0.14%
- Physical form
- Liquid
- Stability
- Tested 2021-04-07; retest 2026-11-28
Contexte d’application
- Thiol-ene materials research: reported in dendrimer-materials work involving terminal-alkene functionality and thiol-ene modification.
- Cross-metathesis chemistry: reported as a terminal-alkene alcohol substrate in Ru-catalyzed cross-metathesis methodology.
- Halocyclization studies: reported in published mechanism studies of terminal alkenyl alcohol halocyclization.
Ressources techniques associées
Sources publiques
- A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems
Journal of the American Chemical Society, 2004
Product-family technical context
- Copper-free click chemistry for dynamic in vivo imaging
Proceedings of the National Academy of Sciences, 2007
Product-family technical context
- A Strain-Promoted [3 + 2] Azide–Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems
Journal of the American Chemical Society, 2004
Product-family technical context
- Tetrazine Ligation: Fast Bioconjugation Based on Inverse-Electron-Demand Diels–Alder Reactivity
Journal of the American Chemical Society, 2008
Product-family technical context
- Composé PubChem 13181
PubChem · CID 13181
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