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N-[2-(2-amino-phenylsulfanyl)-ethyl]-phthalimide is a complex organic compound with the molecular formula C16H14N2O2S. It is characterized by a phthalimide core, which is a cyclic imide derived from phthalic anhydride, and a 2-(2-amino-phenylsulfanyl)-ethyl side chain. The molecule features a sulfanyl group (-SH) attached to a phenyl ring, which is further connected to an ethyl group that links back to the phthalimide. N-[2-(2-amino-phenylsulfanyl)-ethyl]-phthalimide is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is important to note that handling and use of such chemicals should be done with caution, adhering to proper safety protocols, as they can have specific health and environmental considerations.

1157-42-2

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1157-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1157-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1157-42:
(6*1)+(5*1)+(4*5)+(3*7)+(2*4)+(1*2)=62
62 % 10 = 2
So 1157-42-2 is a valid CAS Registry Number.

1157-42-2Relevant academic research and scientific papers

Synthesis of Nickel(II) Complexes of Novel Naphthalimide Based Heterodipodal Schiff Base Ligands, Structure, Characterization and Application for Degradation of Pesticides

Pandiyan, Thangarasu,Raj, Pushap,Sidhu, Jagpreet Singh,Singh, Narinder

, (2020/07/15)

To degrade the highly toxic pesticide into less harmful components, we have synthesized four nickel complexes of naphthalimide based organic ligands. These complexes catalyze the hydrolysis of phosphorothioate bonds of organophosphates in an aqueous medium. The metal complexes {[Ni(L1)2]–[Ni(L4)2]} were synthesized by the electrochemical method and characterized using single-crystal X-ray crystallography and mass spectrometry. Analytical techniques revealed that complexes are mononuclear and possess octahedral geometry. The rate of degradation of chlorpyriphos and parathion methyl was evaluated using 31P NMR and LC-MS chromatogram. The by-product of chlorpyriphos upon catalytic degradation with complex was confirmed from mass spectrometry. It was found that chlorpyriphos degrade into 3,5,6-trichloropyridin-2-ol after 50 minutes of incubation with catalyst. However, parathion methyl took only 20 minutes to hydrolyze into its by-product. Moreover, the inhibition assay of acetylcholinesterase was performed for pesticides in the presence of metal complex and the interesting outcome was recorded.

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