Produktname:N-{[1-(1-benzofuran-2-carbonyl)piperidin-4-yl]methyl}-2,1,3-benzothiadiazole-5-carboxamide
IUPAC Name:N-{[1-(1-benzofuran-2-carbonyl)piperidin-4-yl]methyl}-2,1,3-benzothiadiazole-5-carboxamide
- CAS:1235244-90-2
- Molekulare Formel:C22H20N4O3S
- Reinheit:95%+
- Katalognummer:CM999910
- Molekulargewicht:420.49
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Produkt-Details
- CAS-Nr.:1235244-90-2
- Molekulare Formel:C22H20N4O3S
- Schmelzpunkt:-
- SMILES-Code:O=C(NCC1CCN(CC1)C(=O)C1=CC2=CC=CC=C2O1)C1=CC2=NSN=C2C=C1
- Dichte:
- Katalognummer:CM999910
- Molekulargewicht:420.49
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Category Infos
- 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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- Benzofurans
- Benzofuran is an aromatic heterocyclic organic compound with the chemical formula C8H6O. It is a colorless oily liquid at room temperature with an aromatic odor. Benzofuran can be volatilized with water vapor and can be decomposed by potassium permanganate and other oxidants. It is an intermediate for the preparation of amiodarone and indene resin. Benzofuran derivatives are important pharmaceutical intermediates.
- Benzofuran | C8H6O | CID 9223 -Chemenu
- Benzofuran | C8H6O | CID 9223 |Where to Buy Benzofurans
- Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar.Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.
- Benzothiadiazoles
- The two N atoms in Benzothiadiazole could possibly form intermolecular hydrogen bonding, leading to a more planar backbone. Benzothiadiazole is a strong electron-accepting molecular fragment. By fusing it with thiazole donor-acceptor dyes, near-infrared fluorescence was created. The benzothiadiazole ring is a useful n-type building block for designing electron-transport materials for organic and polymer light-emitting diodes (LEDs). Arene- and heteroarene-fused thiadiazoles have also found use in the design of low-band-gap materials for the construction of organic field-effect transmitters (OFETs), as stable organic radicals, and as one or two photon-absorbing materials for the design of nonlinear near-infrared (NIR) dyes. Benzothiadiazoles acting as the electron-accepting cores have been incorporated into dendrimer-type light-harvesting materials.