cas 1207050-64-3|| where to buy N-[5-(ethylsulfanyl)-1,3,4-thiadiazol-2-yl]-2-(1H-pyrrol-1-yl)-1,3-thiazole-4-carboxamide

Produktname:N-[5-(ethylsulfanyl)-1,3,4-thiadiazol-2-yl]-2-(1H-pyrrol-1-yl)-1,3-thiazole-4-carboxamide

IUPAC Name:N-[5-(ethylsulfanyl)-1,3,4-thiadiazol-2-yl]-2-(1H-pyrrol-1-yl)-1,3-thiazole-4-carboxamide

: CAS：1207050-64-3; Molekulare Formel：C12H11N5OS3; Reinheit：95%+

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: CAS-Nr.:1207050-64-3; Molekulare Formel:C12H11N5OS3; Schmelzpunkt:-; SMILES-Code:CCSC1=NN=C(NC(=O)C2=CSC(=N2)N2C=CC=C2)S1; Dichte:

: Katalognummer:CM994143; Molekulargewicht:337.43; Siedepunkt:; Mdl-Nr.:; Lagerung:

: Pyrroles; Pyrrole is a five membered heterocyclic compound with the molecular formula of C4H5N. Pyrrole has a ring composed of four carbon atoms and one nitrogen atom. Pyrrole is easy to polymerize in the air. Pyrrole is the parent compound of many important biological substances (such as bile pigment, porphyrin and chlorophyll). Pyrrole scaffolds are widely used in biological and pharmaceutical fields. Pyrrole is a special heterocyclic scaffold, which exists in many natural products, drug molecules and pesticides, and has shown its application in materials science.; Pyrrole,Where to Buy Pyrroles-Chemenu; Pyrrole,Where to Buy Pyrroles; Pyrrole is a heterocyclic, aromatic, organic compound, a five-membered ring with the formula C 4H 4NH. It is a colorless volatile liquid that darkens readily upon exposure to air. Substituted derivatives are also called pyrroles, e.g., N-methylpyrrole.

: Thiazoles; Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.

: 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.