Produktname:N-[5-(ethylsulfanyl)-1,3,4-thiadiazol-2-yl]-1-[6-(furan-2-yl)pyridazin-3-yl]piperidine-3-carboxamide
IUPAC Name:N-[5-(ethylsulfanyl)-1,3,4-thiadiazol-2-yl]-1-[6-(furan-2-yl)pyridazin-3-yl]piperidine-3-carboxamide
- CAS：1226450-90-3
- Molekulare Formel：C18H20N6O2S2
- Reinheit：95%+
- Katalognummer：CM642114
- Molekulargewicht：416.52
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Produkt-Details
- CAS-Nr.:1226450-90-3
- Molekulare Formel:C18H20N6O2S2
- Schmelzpunkt:-
- SMILES-Code:CCSC1=NN=C(NC(=O)C2CCCN(C2)C2=CC=C(N=N2)C2=CC=CO2)S1
- Dichte:
- Katalognummer:CM642114
- Molekulargewicht:416.52
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
Category Infos
- Pyridazines
- Pyridazine, also known as o-diazobenzene, is a six-membered heterocyclic compound containing two nitrogen heteroatoms in the 1 and 2 positions with a special structure and a wide biological activity. Pyridazine is more and more popular in drug development, and a variety of pyridazine drugs have been developed and marketed. From the perspective of the therapeutic field, pyridazine drug molecules are mainly used for tumor treatment, but also involve in many therapeutic fields such as inflammation, hypertension and cardiovascular disease. With the increase and in-depth of research, pyridazine drugs will play more roles in the treatment of diseases.
- 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.
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- Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans
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- Piperidines
- Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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- Thiadiazoles
- Thiadiazoles are a subfamily of azoles. Structurally, they are five-membered heterocyclic compounds containing two nitrogen atoms and one sulfur atom, and two double bonds, forming an aromatic ring. Depending on the relative positions of the heteroatoms, there are four possible structures; these forms do not interconvert and are therefore structural isomers rather than tautomers. These compounds themselves are rarely synthesized and have no particular utility, however, compounds that use them as structural motifs are fairly common in pharmacology.
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