Nom du produit:2-(4-hydroxyoxan-4-yl)furan-3-carboxylic Acid
IUPAC Name:2-(4-hydroxyoxan-4-yl)furan-3-carboxylic acid
- CAS：1696992-68-3
- Formule moléculaire：C10H12O5
- Pureté：95%+
- Numéro de catalogue：CM407815
- Poids moléculaire：212.2
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1696992-68-3
- Formule moléculaire:C10H12O5
- Point de fusion:-
- Code SMILES:OC(=O)C1=C(OC=C1)C1(O)CCOCC1
- Densité:
- Numéro de catalogue:CM407815
- Poids moléculaire:212.2
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Furans
- Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.
- Furan | C4H4O | Where to Buy Furans-Chemenu
- Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans
- Looking to buy furan? Chemenu offers a diverse selection of high-quality furan compounds. Find the perfect furans for your research or industrial applications. Explore our inventory today!
- Tetrahydropyrans
- Tetrahydropyran is an organic compound consisting of a saturated six-membered ring containing five carbon atoms and one oxygen atom. Tetrahydropyrans are common structural motifs in natural products and synthetic therapeutic molecules. In nature, these six-membered oxygen heterocycles are usually assembled by intramolecular reactions, including oxygen Michael addition or ring opening of epoxy alcohols. In fact, polyether natural products have been particularly extensively studied for their fascinating structures and important biological properties; these are often formed through endoselective epoxy open cascades.
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