Satranidazole

Analysis Note Assay (HClO&#8324): &#8805 97.0 % Melting range (lower value): &#8805 100 &#176C Melting range (upper value): &#8804 103 &#176C Spec.

Hydrazobenzene has been prepared by the reduction of azobenzene by SmI(2) in THF . Hydrazobenzene is an intermediate in the hydrogenation of azoxybenzene to aniline .

1,3-Di- tert -butylimidazolium tetrafluoroborate is an N -heterocyclic carbene (NHC) compound that can be prepared by reacting paraformaldehyde with tert -butyl amine and hydrogen tetrafluoroborate (35% in water). Application 1,3-Di- tert

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 1,3-Diphenoxybenzene was used: as internal standard during solid-phase extraction and gas chromatography coupled mass spectrometry in the selective ion monitoring (SIM) mode for the multi-class determination of pesticides in the

1,2,4-triethylbenzene

Single-component standards are available as stock items. They are supplied in methanol, or in another solvent, where appropriate.

2,4,6-Tri-tert-butylnitrosobenzene

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

2-amino-6-chloro-benzothiazole on microwave irradiation in the presence of 1-butyl-3-methylimidazolium and inorganic anions yields fluorinated benzothiazolo[2,3-b]quinazoline-2H-ones analogues[1]. It has synergistic effect on inhibitive performance

2-amino-6-chloro-benzothiazole on microwave irradiation in the presence of 1-butyl-3-methylimidazolium and inorganic anions yields fluorinated benzothiazolo[2,3-b]quinazoline-2H-ones analogues[1]. It has synergistic effect on inhibitive performance