AC-12961 - oxalyl-chloride-98 | 75-44-5

<p>Ethyl oxalyl chloride is used in the synthesis of 2-oxo-3-alkenoic esters and alpha-keto ester in good yield. It acts as a reactant in the preparation of oxyoxalamide derivatives as an epoxide hydrolase inhibitor. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar p</p>

<p>Ammonium hexafluorotitanate is used as an anti-corrosive cleaning agent. It is also used for the production of ceramics and glass. Further, it is used in the preparation of synthetic gems. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some do</p>

2H-Indeno[5,4-b]furan-8-ethanamine, 1,6,7,8-tetrahydro-(hydrochloride)(1:1) is a monosubstituted compound that has been synthesized by the Friedel-Crafts reaction. The optical purity of the product was determined to be 98% optically pure with a specific rotation of +30.2 degrees at 20 degrees Celsius. The melting point was found to be 172 degrees Celsius and the boiling point was found to be 296 degrees Celsius. The product can also be synthesized using oxalyl chloride and raney nickel as catalysts in a transfer process. This synthesis can be carried out in two steps: In the first step, 2H-indeno[5,4-b]furan-8-ethanamine is reacted with triazolam (a benzodiazepine) in an oriented synthesis.

<p>Reagent used in organic synthesis. Unncatalyzed reaction of silyl ketene acetals with oxalyl chloride yeilds symmetrical pulvinic acids. Catalytic syntheses of N-heterocyclic ynones and ynediones by in situ activation of carboxylic acids with oxalyl chloride. Oxalyl chloride was reportedly used in t</p>

Oxalyl chloride

<p>Stability Hygroscopic, Moisture Sensitive, Volatile<br>Applications Oxalyl Chloride is used in the preparation of cardiolipin analogs which induce peroxidase activity by Cytochrome C. It is also used in the preparation of fluorescent indicators for cytosolic calcium.<br> E0<br>References Abe, M. et al.: Biochem., 50, 8383 (2011); Minta, A. et al.: J. Biol. Chem., 264, 8171 (1989);<br></p>

Oxalyl chloride is an organic compound that inhibits enzymes whose active site contains a carbonyl group. It is used as an antimicrobial agent in the treatment of bacterial infections, such as urinary tract and respiratory tract infections, and in the manufacture of pharmaceuticals. Oxalyl chloride reacts with diethyl ketomalonate to form oxalyl diethyl ketomalonate, which then undergoes a chemiluminescent reaction with malonic acid. This product has potent antitumor activity and can be used to treat human serum.