3:5‐dinitro‐4‐methyl‐benzazide as a reagent for the identification of phenols
Peter P. T. Sah
Abstract
Peter P. T. Sah
Abstract
Abstract Thirty‐three crystalline urethanes were prepared by the condensation of the new reagent, 3:5‐dinitro‐4‐methyl‐benzazide, in boiling ligroin solution with various phenols. The very high yields of the 3:5‐dinitro‐4‐methylphenyl‐urethanes obtained from the reaction and the excellent properties of these derivatives, indicated that 3:5‐dinitro‐4‐methyl‐benzazide is an excellent micro‐reagent for the identification of phenols.
OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract Thirty‐three crystalline urethanes were prepared by the condensation of the new reagent, 3:5‐dinitro‐4‐methyl‐benzazide, in boiling ligroin solution with various phenols. The very high yields of the 3:5‐dinitro‐4‐methylphenyl‐urethanes obtained from the reaction and the excellent properties of these derivatives, indicated that 3:5‐dinitro‐4‐methyl‐benzazide is an excellent micro‐reagent for the identification of phenols.
Key concepts: Reagent, Phenols, Boiling, Condensation, Chemistry, Phenol, Organic chemistry, Condensation reaction