Cyano-, Nitrile-

<p>Applications 2-Acetyl-4-cyanophenol<br></p>

<p>Applications p-Cyanobenzoic Acid Trimer is used in the synthetic preparation of Terbium Triazinetribenzoate Formate Metal Organic Framework (MOF).<br>References Han, Y., et al.: J. Mater. Chem. A Mater. Energy Sustain., 3, 24525 (2015)<br></p>

<p>Applications Aminoacetonitrile is a useful synthetic intermediate. It is a reagent used to synthesize dipeptide nitriles as reversible and potent cathepsin S inhibitors. It can also used to prepare substituted cyclic ureas as possible HIV protease inhibitors.<br>References Ward, Y., et al.: J. Med. Chem., 45, 5471 (2002); Wilkerson, W., et al.: J. Med. Chem., 40, 4079 (1997)<br></p>

<p>Stability Moisture Sensitive<br>Applications 2-phenyl-2-[(trimethylsilyl)oxy]acetonitrile (cas# 25438-37-3) is a useful research chemical.<br></p>

<p>Applications Cyanomethyl Methyl(phenyl)carbamodithioate (cas# 76926-16-4) is a useful research chemical.<br></p>

<p>Applications (3,5-Dimethoxyphenyl)acetonitrile (cas# 13388-75-5) is a compound useful in organic synthesis.<br></p>

<p>Applications N-​(4-Cyanophenyl)​-6-​benzothiazolecarboxa​mide is a compound used in the synthesis of piperazines presenting neuro and psychotropic agent with low toxicity.<br></p>

<p>Applications BENZYL CYANOMETHYLCARBAMATE (cas# 3589-41-1) is a useful research chemical.<br></p>

<p>Potassium tetracyanoaurate(III) (K[AuCl4]) is a crystalline, intermetallic compound that has been used in the production of coatings, spherical particles, and electrochemical materials. The pentahydrate form has a diameter of 4.8-5.2 Å and a melting point of ~115°C. K[AuCl4] is stable in air and water but reacts with strong acids to form potassium chloride and potassium tetracyanocuprate(II). This substance also has an optimal pH range of 6-7 and an average solubility range of 0.05-0.1g/100mL at 20°C. The microstructure of K[AuCl4] is not well understood because it is difficult to isolate from other compounds during synthesis.</p>

<p>4-Fluoro-3-nitrophenylacetonitrile is a monomer that can be synthesised from the reaction of carbamic acid and diphenyl ether. It is chiral, stereoselective and nucleophilic. 4-Fluoro-3-nitrophenylacetonitrile can also be synthesised by reacting fluoroacetamide with sodium cyanide in water, forming the corresponding amide, which reacts with acetonitrile to form the nitro compound. The anti-cancer properties of 4-fluoro-3 nitrophenylacetonitrile have been studied in vitro and in vivo. This substance has been shown to inhibit growth of cancer cells and induce apoptosis. In addition, this substance has been used as a synthetic strategy for dihydroisoquinolines, which are important for their anti-cancer properties.</p>

<p>Please enquire for more information about N-Cyano-N',S-dimethylisothiourea including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Cyanobenzenecarboximidamide hydrochloride (NCBCH) is an intermediate for the synthesis of azomethine dyes. It can be used to produce azo dyes with a methoxy group at the 3 position and a hydrogen atom at the 4 position. NCBCH is also an excellent substrate for chemical reactions involving fragmentation, extraction, or elimination. NCBCH can be synthesized from methyl ether and benzonitrile in the presence of benzamidine. The product is then treated with methanol to give a tautomeric mixture of benzyl and methyl ether.</p>

<p>Please enquire for more information about Methyl-2-isocyanoisobutyrate 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 1-Methylindole-3-acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>