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2-(4-chlorophenyl)acetohydroxamic acid is an organic compound with the chemical formula C8H8ClNO2. It is a derivative of acetohydroxamic acid, featuring a 4-chlorophenyl group attached to the acetohydroxamic acid structure. 2-(4-chlorophenyl)acetohydroxamic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain herbicides and pesticides. Its chemical properties include the ability to form chelates with metal ions, which is a characteristic feature of hydroxamic acids. The compound is typically synthesized through a reaction involving 4-chlorobenzaldehyde and hydroxylamine, followed by a reduction step. Due to its reactivity and potential applications, 2-(4-chlorophenyl)acetohydroxamic acid is an important molecule in the field of organic chemistry and chemical engineering.

2593-91-1

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2593-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2593-91-1 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, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2593-91:
(6*2)+(5*5)+(4*9)+(3*3)+(2*9)+(1*1)=101
101 % 10 = 1
So 2593-91-1 is a valid CAS Registry Number.

2593-91-1Downstream Products

2593-91-1Relevant academic research and scientific papers

N-hydroxy-substituted 2-aryl acetamide analogs: A novel class of HIV-1 integrase inhibitors

Debnath, Utsab,Kumar, Prachi,Agarwal, Aakanksha,Kesharwani, Ajay,Gupta, Satish K.,Katti, Seturam B.

, p. 527 - 534 (2017)

An in silico method has been used to discover N-hydroxy-substituted 2-aryl acetamide analogs as a new class of HIV-1 integrase inhibitors. Based on the molecular requirements of the binding pocket of catalytic active site, two molecules (compounds 2 and 4

A two-step tandem reaction to prepare hydroxamic acids directly from alcohols

Dettori, Giovanna,Gaspa, Silvia,Porcheddu, Andrea,De Luca, Lidia

supporting information, p. 4582 - 4585 (2014/06/24)

The first synthesis of hydroxamic acids from alcohols has been developed. Both benzylic and aliphatic alcohols can be tolerated and applied in this reaction. The methodology is economical, environmentally benign and high yielding. This journal is

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