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Sulfamide, N-butyl-N'-cyclohexyl-, also known as N-butyl-N'-cyclohexylsulfamide or BCS, is an organic compound with the chemical formula C12H25NO2S. It is a white crystalline solid that is soluble in water and various organic solvents. BCS is primarily used as a corrosion inhibitor in industrial applications, particularly in the oil and gas industry, where it helps to prevent the formation of scale and corrosion in pipelines and equipment. Additionally, it has been studied for its potential use as a flame retardant and as a component in various chemical formulations. The compound is synthesized through the reaction of butylamine and cyclohexylamine with sulfuric acid, and its properties, such as its ability to form complexes with metal ions, contribute to its effectiveness in these applications.

3488-39-9

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3488-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3488-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3488-39:
(6*3)+(5*4)+(4*8)+(3*8)+(2*3)+(1*9)=109
109 % 10 = 9
So 3488-39-9 is a valid CAS Registry Number.

3488-39-9Downstream Products

3488-39-9Relevant academic research and scientific papers

Hypervalent iodine reagent mediated diamination of [60]fullerene with sulfamides or phosphoryl diamides

Yang, Hai-Tao,Lu, Xin-Wei,Xing, Meng-Lei,Sun, Xiao-Qiang,Miao, Chun-Bao

supporting information, p. 5882 - 5885 (2015/02/19)

A hypervalent iodine-promoted intermolecular diamination reactions of C60 with sulfamides or phosphoryl diamides affords two classes of novel C60-fused cyclic sulfamide or phosphoryl diamide derivatives. The reaction between C60 and sulfamides can be effectively controlled to selectively synthesize diamination products or azafulleroids under PhIO/I2 or PhI(OAc)2/I2 conditions, respectively. Moreover, phosphoryl diamides were first used as an amine source in the diamination of alkenes.

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