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4-chloro-N-((methylsulfonyl)oxy)benzimidoyl chloride is a chemical compound with the molecular formula C9H7ClN2O3S. It is a derivative of benzimidoyl chloride, featuring a 4-chloro substitution on the benzene ring and a methylsulfonyl group attached to the nitrogen atom. 4-chloro-N-((methylsulfonyl)oxy)benzimidoyl chloride is known for its reactivity and is often used as a reagent in organic synthesis, particularly in the formation of amides and other nitrogen-containing compounds. Its structure allows it to act as a chlorinating and sulfonylating agent, making it a versatile tool in the creation of complex molecules. Due to its reactivity, it is typically handled with care in a laboratory setting.

5023-88-1

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5023-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5023-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5023-88:
(6*5)+(5*0)+(4*2)+(3*3)+(2*8)+(1*8)=71
71 % 10 = 1
So 5023-88-1 is a valid CAS Registry Number.

5023-88-1Relevant academic research and scientific papers

One-pot synthesis of trisubstituted ureas from achloroaldoxime O-methanesulfonates and secondary amines

Kaeobamrung, Juthanat,Lanui, Asan,Mahawong, Sirinad,Duangmak, Witthawin,Rukachaisirikul, Vatcharin

, p. 58587 - 58594 (2018/02/19)

Trisubstituted ureas can be synthesized in a one-pot fashion from bench-stable a-chloroaldoxime Omethanesulfonates and secondary amines under mild reaction conditions. Two practical protocols have been developed to achieve various urea syntheses from both secondary aromatic amines and aliphatic amines.

N-(sulfonyloxy) benzimidoyl halides as bactericidal or fungicidal agents

-

, (2008/06/13)

Agricultural fungicidal compositions based on N-(sulfonyloxy)benzimidoyl halides exhibit a broad spectrum of antifungal activity, particularly against late blight, bean rust and rice blast. The synthesis of representative compounds is described, and the utility of antifungal compositions is exemplified.

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