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2-Chlor-phenyl-acethydroxamsaeure, also known as 2-chlorophenyl acetohydroxamic acid, is an organic compound with the chemical formula C8H8ClNO2. It is a derivative of acetohydroxamic acid, featuring a 2-chlorophenyl group attached to the acetic acid moiety. <2-Chlor-phenyl>-acethydroxamsaeure is of interest in chemical research and may have potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure. It is typically synthesized through the reaction of 2-chlorobenzoic acid with hydroxylamine, and its properties, such as reactivity and stability, are influenced by the presence of the chlorine atom on the phenyl ring.

2593-89-7

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2593-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2593-89-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2593-89:
(6*2)+(5*5)+(4*9)+(3*3)+(2*8)+(1*9)=107
107 % 10 = 7
So 2593-89-7 is a valid CAS Registry Number.

2593-89-7Downstream Products

2593-89-7Relevant academic research and scientific papers

A convenient method for the preparation of hydroxamic acids

Reddy,Kumar,Reddy

, p. 6285 - 6288 (2000)

A one-step conversion of carboxylic acid to hydroxamic acid, under neutral pH conditions is described. This simple, selective and efficient method was applied to a wide range of aliphatic/aromatic carboxylic acid derivatives that contain hydroxyl, halo, ester and other base sensitive groups as substituents. The method utilizes cheaply available reagents and hence it is a practical and cost effective strategy, compared to the other methods available in the literature. (C) 2000 Elsevier Science Ltd.

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