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Benzolsulfonsaeure-<β-anilino-tert-butylamid>, also known as benzenesulfonic acid β-anilino-tert-butylamide, is a complex organic compound with the chemical formula C14H18N2O3S. It is a derivative of benzenesulfonic acid, featuring an amide group attached to the β-position of the aniline moiety, with a tert-butyl group providing steric hindrance. Benzolsulfonsaeure-<β-anilino-tert-butylamid> is characterized by its white crystalline appearance and is soluble in organic solvents. It is synthesized through a series of chemical reactions involving the coupling of benzenesulfonic acid with the appropriate aniline and tert-butylamine derivatives. Benzolsulfonsaeure-<β-anilino-tert-butylamid> has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various drugs and other organic compounds. Its specific uses and properties are subject to ongoing research and development.

2951-59-9

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2951-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2951-59-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2951-59:
(6*2)+(5*9)+(4*5)+(3*1)+(2*5)+(1*9)=99
99 % 10 = 9
So 2951-59-9 is a valid CAS Registry Number.

2951-59-9Downstream Products

2951-59-9Relevant academic research and scientific papers

Aziridines, 61 +"--"+ Ring Opening of 2,2-Dimethyl-1-sulfonylaziridines by Anilines: Regioselectivity and Revised Structure of Main Products

Buchholz, Berthold,Lin, Pen-Yuan,Onistschenko, Andreas,Stamm, Helmut

, p. 483 - 487 (2007/10/02)

It is shown (1) that in the most reactions of anilines 2 with 1-sulfonyl-2,2-dimethylaziridines 1 both isomeric products 3 and 4 are formed, (2) that the "normal" product 4 obtained by attack on position 3 of 1 usually arises in a small or negligible amount that seems to decrease with decreasing basicity of 2, and (3) that the amount of 4 strongly increases with increasing steric demand of 2.Formation of 4 is explained by a lag of bond making in SN2. +"--"+ N-Aryl-N'-sulfonyl-gem-dimethylethylenediamines, 1-Sulfonyl-2,2-dimethylaziridines, Regioselectivity of Nucleophilic Ring Opening, Steric Hindrance Effect, Basicity Effect

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