Название продукции:N-[1-(thiophen-2-yl)cyclopentyl]-2,1,3-benzothiadiazole-4-sulfonamide

IUPAC Name:N-[1-(thiophen-2-yl)cyclopentyl]-2,1,3-benzothiadiazole-4-sulfonamide

CAS:2034384-03-5
Молекулярная формула:C15H15N3O2S3
Чистота:95%+
Номер в каталоге:CM979934
Молекулярная масса:365.48

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Номер CAS:2034384-03-5
Молекулярная формула:C15H15N3O2S3
Точка плавления:-
Smiles-код:O=S(=O)(NC1(CCCC1)C1=CC=CS1)C1=CC=CC2=NSN=C12
Плотность:
Номер в каталоге:CM979934
Молекулярная масса:365.48
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
Cyclopentanes
Cyclopentane is a cycloalkane, an organic compound with a molecular formula of C5H10, a colorless and transparent liquid, insoluble in water, soluble in most organic solvents such as ethanol, ether, benzene, carbon tetrachloride, acetone, etc. It is mainly used as a solvent and chromatographic reference materials.
Cyclopentanes,where to buy Cyclopentanes
Cyclopentanes
Cyclopentane (also called C pentane) is a highly flammable alicyclic hydrocarbon with chemical formula C5H10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It occurs as a colorless liquid with a petrol-like odor.
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.

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