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N'-Cyclobutylidene-4-methylbenzenesulfonohydrazide is a chemical compound with the molecular formula C12H15N3O2S. It is a derivative of benzenesulfonohydrazide, featuring a cyclobutylidene group attached to the nitrogen atom. N'-cyclobutylidene-4-methylbenzenesulfonohydrazide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically used as an intermediate in the preparation of more complex molecules, particularly those involving the formation of heterocyclic rings. The compound's properties, such as its solubility and stability, can be influenced by the presence of the cyclobutylidene group, making it a valuable building block in organic synthesis.

2524-51-8

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2524-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2524-51-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2524-51:
(6*2)+(5*5)+(4*2)+(3*4)+(2*5)+(1*1)=68
68 % 10 = 8
So 2524-51-8 is a valid CAS Registry Number.

2524-51-8Relevant academic research and scientific papers

Regioselective preparation of saturated spirocyclic and ring-expanded fused pyrazoles

Merchant, Rohan R.,Allwood, Daniel M.,Blakemore, David C.,Ley, Steven V.

, p. 8800 - 8811 (2014)

Saturated bicyclic pyrazoles represent an important class of biologically active molecules, but their preparation can be hampered by labor-intensive synthesis of required starting materials. A convenient one- or two-step procedure for the synthesis of sat

Palladium-Catalyzed Carbene Coupling Reactions of Cyclobutanone N-Sulfonylhydrazones

Ning, Xiaoqin,Chen, Yongke,Hu, Fangdong,Xia, Ying

supporting information, p. 8348 - 8352 (2021/10/25)

Described herein are the palladium-catalyzed cross-coupling reactions of cyclobutanone-derived N-sulfonylhydrazones with aryl or benzyl halides, suggesting that the metal carbene process and β-hydride elimination can smoothly occur in strained ring system

Reaction of Substituted Hydrazones with Thionyl Chloride and Sulfuryl Chloride

Meier, Herbert,Trickes, Georg,Laping, Elisabeth,Merkle, Ursula

, p. 183 - 192 (2007/10/02)

Treatment of acetylhydrazones 2, ethoxycarbonylhydrazones 3, p-tolylsulfonylhydrazones 4 or semicarbazones 5 with thionyl chloride leads to the 1,2,3-thiadiazoles 6a-o.Sulfuryl chloride on the other hand accomplishes the transfer of chlorine without incorporating a sulfur atom.The new synthesized 1,2,3-thiadiazoles 6g-o are characterized in detail by spectroscopic methods.

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