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"2-{[4-(4-methylphenyl)-5-phenyl-4H-1,2,4-triazol-3-yl]sulfanyl}-1-(3-nitrophenyl)ethanone" is a complex organic compound with the molecular formula C21H17N3O4S. It features a 1,2,4-triazole ring system, which is a five-membered heterocyclic ring containing three nitrogen atoms. The triazole ring is fused to a phenyl group at the 5-position and is substituted with a 4-methylphenyl group at the 4-position. The compound also contains a sulfanyl group (-SH) attached to the triazole ring, which can potentially form disulfide bonds with other molecules. Additionally, it has a 3-nitrophenyl group attached to the ethanone (keto) group, which contributes to its reactivity and chemical properties. 2-{[4-(4-methylphenyl)-5-phenyl-4H-1,2,4-triazol-3-yl]sulfanyl}-1-(3-nitrophenyl)ethanone may have potential applications in the fields of pharmaceuticals, materials science, or as a chemical intermediate due to its unique structure and reactivity.

6558-57-2

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6558-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6558-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6558-57:
(6*6)+(5*5)+(4*5)+(3*8)+(2*5)+(1*7)=122
122 % 10 = 2
So 6558-57-2 is a valid CAS Registry Number.

6558-57-2Downstream Products

6558-57-2Relevant academic research and scientific papers

Formation of Halide Complexes of Methyl- and Inorganic Germanium(IV) in Aqueous Hydrohalogenic Acid Solutions

Sohrin, Yoshiki

, p. 3363 - 3371 (2007/10/02)

The reaction of methyl- and inorganic germanium(IV) hydroxides ((CH3)nGe(OH)4-n; n = 1, 2, or 3) with halide ions (X = Cl-, Br-, or I-) to form halide complexes ((CH3)nGeX4-n) in aqueous acidic solution has been investigated by liquid-liquid extraction, solid-liquid distribution (ion exchange), and 1H NMR spectrometry.It has been found that methylgermanium moieties are hard Lewis acids similarly to inorganic germanium(IV), because the stability constant of the halide complexes decreases in the order Cl- > Br- > I-.The stability constant for an X- ion increases as the number of methyl groups attached to the germanium atom increases.The species of inorganic-, monomethyl-, and dimethylgermanium are nonionic and have a tetrahedral structure in HX solution, and OJ- ions attached to the germanium atom are stepwise substituted by X- ions with an increase in HX activity.Trimethylgermanium alone forms a cation, when the activity of HX is not sufficiently high.These facts suggest that the transfer of a negative charge from methyl groups to the central germanium atom lowers the stability of the bond between the germanium atom (hard acid) and an OH- ion (hard base).

Direct Synthesis of Organobromogermanes from Methylenebromide

Schmidbaur, Hubert,Rott, Johann

, p. 285 - 287 (2007/10/02)

From the copper-catalyzed reaction of germanium powder with dibromomethane at 310 deg C a mixture of alkylbromogermanes is obtained.The major products are CH3GeBr3, Br3GeCH2Br (1), CH2(GeBr3)2 (2) and (CH2GeBr2)3 (3).The product distribution parallels the analogous reaction with dichloromethane reported previously.All compounds were characterized by analytical and spectroscopic data, and can be converted into the corresponding hydrides. - Keywords: Alkylbromogermanes, Synthesis, CVD Feeding Gas, Germanium/Copper Mixtures

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