Cyano-, Nitrile-

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

<p>Applications Methyl 2-cyanobenzoate<br></p>

<p>Applications Used as a building block for the preparation of 4H-pyrans, 2-pyridones, furans and carbocyclics.<br>References Herschhorn, A., et al.: J. Med. Chem., 50, 3402 (2007),<br></p>

<p>Impurity Proguanil EP Impurity A<br>Applications 1-Cyano-3-isopropylguanidine (Proguanil EP Impurity A) is an intermediate commonly used for the synthesis of guanide derivatives.An Impurity in the synthesis of Chlorguanide (C329500).<br>References Jensen, N., et al.: J. Med. Chem., 44, 3925 (2001), Paci, A., et al.: J. Pharm. Biomed. Anal., 27, 1 (2002),<br></p>

<p>Applications An intermediate for insecticide.<br>References Cole, L., et al.: Pestic. Biochem. Physiol., 46, 47 (1993), Cole, L., et al.: Life Sci., 56, 757 (1995), Hosie, A., et al.: Br. J. Pharmacol., 115, 909 (1995),<br></p>

<p>Stability Air Sensitive, Light Sensitive<br>Applications 2-Amino-4-cyano-phenol<br></p>

<p>Applications Methyl 3-Cyanoropionate is used in the preparation of anticancer agents. Also used in the design of the ‘dipeptoid’ analogs of cholecystokinin.<br>References Graham, L. et al.: J. Med. Chem., 55, 7817 (2012); Boden, P. et al.: Eur. J. Med. Chem., 28, 47 (1993);<br></p>

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

<p>Applications 3-Cyanobenzoic Acid, is a building block used for the synthesis of a variety of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids, that can be used for the synthesis of a metabotropic glutamate subtype 5 (mGlu5) receptor antagonist.<br>References Ramu, T., et al.: Chem. Lett., 42, 722 (2013);<br></p>

<p>(1-Methyl-1H-benzoimidazol-2-yl)-acetonitrile is a nucleophilic compound that reacts with carbanions to form alkyl benzoates. It can also act as an electrophile in the formation of nitroalkenes and amides, as well as an intermediate in the synthesis of phenazines. The potassium salt of this compound is used as a reagent in organic synthesis. (1-Methyl-1H-benzoimidazol-2-yl)-acetonitrile has been shown to react with methylene and aromatize to produce ethyl cyanoacetate, which can be used for the production of malononitrile. This reaction is catalyzed by potassium carbonate and esters.</p>

<p>Diethyl cyanophosphonate is a compound that is used as a fluorescence probe for amides and pyrazole rings. It binds to the ester form of the amide, which can then be detected with a fluorescence detector. The chemical reaction between diethyl cyanophosphonate and the ester form is reversible, so it can be used as a hypoglycemic agent. Diethyl cyanophosphonate has potent antitumor activity and binds to nerve cells, causing them to become electrically active.</p>

<p>Please enquire for more information about 3-Cyanothiophene-4-boronic acid pinacol ester 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-Cyano-N-cyclohexyl-N-methylacetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-6-cyanopyrazine is a compound that has been shown to have antimycobacterial activity against Mycobacterium avium. It may also have tuberculostatic activity and be useful for the treatment of tuberculosis. 2-Chloro-6-cyanopyrazine inhibits bacterial growth by binding to DNA, RNA, and protein synthesis in mycobacteria. The antibacterial effect is due to its ability to inhibit amidation and alkylation reactions, as well as its nucleophilic properties. 2-Chloro-6-cyanopyrazine is an acidic compound with a pKa of 3.2, which makes it more soluble in water than hydrophobic compounds such as alkanoic acids.</p>

<p>Dimethylcyanamide is an organic compound that can be synthesized from cyanide or cyanic acid. Dimethylcyanamide is a colorless liquid with a strong odor. It has been used in the past as a precursor to other compounds, but it has since been replaced by cheaper and more convenient methods. Dimethylcyanamide reacts with primary amines to form nitriles, which are useful intermediates in organic synthesis. In addition, the reaction of dimethylcyanamide with secondary amines leads to the formation of primary amines. The transamination of dimethylamine-N-oxide yields a-dimethylaminopropionitrile as an intermediate product. The elimination reaction mechanism for this process involves the conversion of ammonia into hydroxide ions and hydrogen gas. This reaction produces high yields for both products and does not require high temperatures or pressures.</p>

<p>5-Cyanopyridine-2-carboxylic acid is a small molecule that has been found to have significant biological activity in a number of different areas, including neurotherapeutics. It is the result of a scalable synthesis and is soluble in water. The molecule has two chiral centers and can exist as four different stereoisomers (enantiomers). In vitro studies show that 5-cyanopyridine-2-carboxylic acid inhibits fatty acid uptake by blocking the proton pump, which transports lipids into cells. This compound also binds to the cytosolic protein pyrazine 2-carboxylic acid receptor 1 (PYZR1), which may provide an explanation for its effects on fatty acid uptake.</p>