CAS 83-01-2: N,N-Diphenylcarbamic chloride

Diphenylcarbamyl Chloride

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aromatic cyclic amides (including cyclic carbamates) an

Diphenylcarbamyl chloride is a hydrogen-bond inhibitor that binds to the viral envelope protein, interfering with its function. It has been shown to inhibit the activity of certain viruses, including influenza virus and herpes simplex virus. Diphenylcarbamyl chloride also inhibits the enzyme trypsin in soybean extracts, which may be due to its ability to form a hydrogen bond with the hydroxyl group on tyrosine. This drug inhibits the synthesis of proteins in cells by binding to phospholipids on the cell membrane and blocking the passage of amino acids into the cells. The optimum pH for diphenylcarbamyl chloride is between 7 and 8, and it is soluble in water or organic solvents. Diphenylcarbamyl chloride can be synthesized from phosphorus pentoxide and phenylamine.

Diphenylcarbamoyl chloride was used to isolate peptido-keratan sulphate fragments from bovine intervertebral discs. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Impurity Temozolomide USP Related Compound C Applications N,N-Diphenylcarbamyl Chloride (Temozolomide USP Related Compound C) is used in the production of a high performance polyamide used as an electrical switch for memory devices. Also used in the synthesis of modified oligoribonucleotides base pairs. References Hahm, S. et al.: J. Mat. Chem., 19, 2207 (2009); Koga, Y. et al.: Nucl. Nucleo. Nucleic. Acids, 32, 124 (2013);