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N-benzyl-4-nitrobenzenesulfenamide is an organic compound with the chemical formula C13H12N2O3S. It is a derivative of benzenesulfenamide, featuring a nitro group at the para position and a benzyl group attached to the nitrogen atom. This yellow crystalline solid is known for its reactivity and is often used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the development of new compounds with potential applications in various industries.

5147-65-9

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5147-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5147-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5147-65:
(6*5)+(5*1)+(4*4)+(3*7)+(2*6)+(1*5)=89
89 % 10 = 9
So 5147-65-9 is a valid CAS Registry Number.

5147-65-9Downstream Products

5147-65-9Relevant academic research and scientific papers

N-trifluoroacetyl arenesulfenamides, effective precursors for synthesis of unsymmetrical disulfides and sulfenamides

Bao, Ming,Shimizu, Masao

, p. 9655 - 9659 (2003)

N-Trifluoroacetyl arenesulfenamides (3) were effective precursors for the synthesis of unsymmetrical disulfides (4) and sulfenamides (5). Reactions of 3 with a variety of aromatic thiols at room temperature were generally complete within 5 min and gave unsymmetrical diaryl disulfides in high yields. Aralkyl disulfides were isolated in high yields from the reaction of 3 with aliphatic thiols. The nucleophilic substitution reactions of 3 with amines proceeded smoothly and provided N-substituted sulfenamides in good to excellent yields.

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