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2-(4-aminobenzenesulfonylamido)-5-methylthio-1,3,4-thiadiazole is a complex organic chemical compound with the molecular formula C9H8N4O2S3. It is characterized by a 1,3,4-thiadiazole ring system, which is a five-membered ring containing three sulfur atoms and one nitrogen atom. The compound features a 4-aminobenzenesulfonyl group attached to the 2-position of the thiadiazole ring, which contributes to its reactivity and potential applications. The 5-position of the thiadiazole ring is substituted with a methylthio group, further enhancing its chemical properties. 2-(4-aminobenzenesulfonylamido)-5-methylthio-1,3,4-thiadiazole is of interest in the field of organic chemistry, particularly for its potential use in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity.

5684-77-5

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5684-77-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5684-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5684-77:
(6*5)+(5*6)+(4*8)+(3*4)+(2*7)+(1*7)=125
125 % 10 = 5
So 5684-77-5 is a valid CAS Registry Number.

5684-77-5Downstream Products

5684-77-5Relevant academic research and scientific papers

Ultrasound accelerated sulfonylation of amines by p-acetamidobenzenesulfonyl chloride using Mg–Al hydrotalcite as an efficient green base catalyst

Truong, Binh Nhat,Le, Luong Huu,Chau, Duy-Khiem Nguyen,Duus, Fritz,Luu, Thi?Xuan?Thi

, p. 515 - 528 (2016/10/03)

The sulfonylation reaction of various aliphatic, alicyclic, aromatic, and hetero-aromatic amines with p-acetamidobenzenesulfonyl chloride has been investigated using different types of base catalysis under varied reaction conditions. Mg–Al hydrotalcite, characterizable as an inexpensive, reusable, and green solid catalyst, was found to be the most efficient catalyst, when the reaction is carried out in a minimum volume of solvent (acetone). The reaction was found to be accelerated drastically with the support of ultrasound irradiation, affording the sulfonamides in yields better or equivalent to those obtained under the longer lasting conventional stirring conditions.

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