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Carbamimidic acid, hydroxy-, 4-chlorophenyl ester is a chemical compound with the molecular formula C7H6ClN3O3. It is an ester derivative of hydroxycarbamimidic acid, featuring a 4-chlorophenyl group attached to the hydroxyl group. Carbamimidic acid, hydroxy-, 4-chlorophenyl ester is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Its chemical structure consists of a carbamic acid group, a hydroxyl group, and a 4-chlorophenyl ester group, which contribute to its reactivity and utility in chemical reactions. The compound is typically synthesized through the reaction of hydroxycarbamimidic acid with 4-chlorophenol in the presence of a suitable coupling agent. Due to its potential applications in the pharmaceutical and agrochemical industries, research on its properties and reactions is of significant interest to chemists and biologists.

3174-95-6

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3174-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3174-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3174-95:
(6*3)+(5*1)+(4*7)+(3*4)+(2*9)+(1*5)=86
86 % 10 = 6
So 3174-95-6 is a valid CAS Registry Number.

3174-95-6Relevant academic research and scientific papers

Compositions and Methods for Controlling Nematodes

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Page/Page column 34, (2010/08/22)

Compositions and processes for controlling nematodes are described herein, e.g., nematodes that infest plants or animals. The compounds include oxazoles, oxadiazoles and thiadiazoles.

Interaction of aryloxychlorocarbenes with acetylenedicarboxylate: Novel formation of polyfunctional butadienes and 8-oxatricyclo[3.2.1.0 2.4]oct-6-enes

Cheng, Ying,Zhu, Qing,Li, Quan Song,Meth-Cohn, Otto

, p. 4840 - 4846 (2007/10/03)

The interaction of aryloxychlorocarbenes with dialkyl acetylenedicarboxylates has been examined. Thermolyses of 3-aryloxy-3- chlorodiazirines in the presence of acetylenedicarboxylate resulted in the formation of unexpected polyfunctional 1,3-butadienes and 8-oxatricyclo[3.2.1. 02.4]oct-6-enes or of 2-aryoxycarbonylmaleates dependent upon reaction conditions. This work confirmed the nucleophilicity of aryloxychlorocarbenes and underlined their synthetic potential.

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