4-Pentynoic acid
pent-4-ynoic acid
Résumé du produit
Aperçu rapide
- Famille de produits
- Click Chemistry & Bioconjugation Reagents
- Nom chimique
- pent-4-ynoic acid
- FM
- C5H6O2
- PM
- 98.1
- Pureté
- >98.0% (GC, titration)
4-Pentynoic acid is a terminal alkyne carboxylic acid also indexed as pent-4-ynoic acid and propargylacetic acid.
CH63006 is listed with CAS 6089-09-4, molecular formula C5H6O2, and molecular weight 98.1. Research literature links 4-Pentynoic acid with copper(I)-catalyzed cyclization, click-controlled cyclodextrin stationary phases, dihydrodipyrrin building-block synthesis, and chemoselective alkyne-azide oligomer chemistry.
Identité et spécifications
| Catalog No. | CH63006 |
| CAS No. | 6089-09-4 |
| Chemical Name | pent-4-ynoic acid |
| Molecular Formula | C5H6O2 |
| Molecular Weight | 98.1 |
| PubChem CID | 22464 |
| InChIKey | MLBYLEUJXUBIJJ-UHFFFAOYSA-N |
| Purity | >98.0% (GC, titration) |
Conditions de stockage
0-10 C
Caractéristiques techniques
- Building-block class
- Terminal-alkyne carboxylic acid
- Reactive handle
- Terminal alkyne
- Complementary handle
- Carboxylic acid
- Supported chemistry
- Azide-alkyne click and chemoselective construction
- Packaging
- 1 g; 5 g; Custom packaging on request
- Physical form
- Solid
Contexte d’application
- Copper-catalyzed cyclization: reported as a terminal alkyne carboxylic acid substrate in copper(I)-catalyzed cyclization research.
- Click-controlled stationary phases: reported as an acidic alkyne moiety in cyclodextrin chiral stationary phase preparation.
- Building-block synthesis: reported in organic synthesis literature connected to dihydrodipyrrin building-block preparation.
- Alkyne-azide oligomer chemistry: relevant to chemoselective oligomer construction using alkyne-azide cycloaddition chemistry.
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 22464
PubChem · CID 22464
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