≥98% pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.
Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.
SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.
Cité dans 2 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.
4-Methoxypyridine has been prepared from 4-methoxypyridine-N-oxide, via catalytic hydrogenation. Ortho lithiation of 4-methoxypyridine using mesityllithium as the metalating base has been studied.
Used in an efficient construction of dihyropyridin-4-ones potential ligands for neuronal nicotinic acetycholine receptors.
Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.
<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.
Rechercher le COA →Résumé de référence rapide des spécifications et applications du produit.
Voir la fiche technique →Attributs de qualité complets et critères d'acceptation pour cette qualité.
Voir la fiche de spécifications →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Ethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alkyl aryl ethers |
| Alternative Parents | Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Alkyl aryl ether - Pyridine - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as alkyl aryl ethers. These are organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 G2613008 | Certificate of Analysis | Jul 20, 2026 | M120571 |
| F2630082 | Certificate of Analysis | Jul 04, 2026 | M120571 |
| A2122375 | Certificate of Analysis | Dec 16, 2024 | M120571 |
| A2629031 | Certificate of Analysis | Jun 21, 2022 | M120571 |
| E2526064 | Certificate of Analysis | Jun 21, 2022 | M120571 |
| I2202612 | Certificate of Analysis | Jun 21, 2022 | M120571 |
| I2202614 | Certificate of Analysis | Jun 21, 2022 | M120571 |
| I2202615 | Certificate of Analysis | Jun 21, 2022 | M120571 |
| Indice de réfraction | 1.521 |
|---|---|
| Point d'éclair (°F) | 165.2 °F |
| Point d'éclair (°C) | 74°(165°F) |
| Point d'ébullition (°C) | 191°C |
| Point de fusion (°C) | 4°C |
| Poids moléculaire | 109.130 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 109.053 Da |
| Monoisotopic Mass | 109.053 Da |
| Topological Polar Surface Area | 22.100 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 59.500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 |
