Idrazine

<p>Please enquire for more information about 1-methyl-N-[3-(trifluoromethyl)phenyl]-1-hydrazinecarbothioamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-((4-Chlorophenyl)sulfonyl)-3-hydrazinoprop-2-enenitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Applications o-Tolylhydrazine Hydrochloride is a reagent used in the organic syntheses such as opioid receptor antagonists as well as adenosine receptor antagonists as well as adenosine receptor antagonists.<br>References Colotta, V. et al.: J. Med. Chem., 43, 3118 (2000); Portoghese, P. et al.: J. Med. Chem., 33, 1714 (1990);<br></p>

<p>Applications 2-(diphenylacetyl)-3-hydrazino-1H-Inden-1-one is a useful chemical reagent.<br></p>

<p>Applications N-Trifluoroacetyl-N’-thioformamidohydrazine (cas# 51321-51-8) is a compound useful in organic synthesis.<br></p>

<p>Applications N-Nitroso-2,2’-iminodiacetohydrazide (~80%) is a useful research chemical, a potential anticancer compound.<br>References Zimmer, H., et al.: Ohio J. Sci., 59, 327 (1959)<br></p>

<p>Applications ALLYLHYDRAZINE DIHYDROCHLORIDE (cas# 70629-62-8) is a useful research chemical.<br></p>

<p>Applications [4-(Difluoromethoxy)phenyl]hydrazine is used as a reagent in the synthesis of dihydropyrazolopyridinones as functionally selective benzodiazepine binding site ligands on the GABAA receptor.<br>References Mitchinson, A., et al.: Bioorg. Med. Chem. Lett., 14, 3441 (2004)<br></p>

<p>Stability Not determined<br>Applications 2-Hydroxyethylhydrazine is a reagent that is used in the preparation of dichlorophenoxymethyl-substituted pyrazolones and analogs as neuroprotectors against cytoxicity from protein aggregation of mutant superoxide dismutase 1.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Trippier, P. C., et al.: Bioorg. Med. Chem. Lett., 22, 6647 (2012); Rothstein, J., et al.: Anal. Nuerol, 65, S3 (2009)<br></p>