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(E)-1-methoxycarbonyl-2-phenylsulphinylhex-1-ene is a complex organic compound characterized by a hexene backbone with a methoxycarbonyl group at the 1-position and a phenylsulphinyl group at the 2-position. The molecule exhibits a trans (E) configuration, indicating that the substituents at the double bond are on opposite sides. The methoxycarbonyl group is an ester derivative, while the phenylsulphinyl group introduces a sulfur atom bonded to a phenyl ring, which can influence the compound's reactivity and properties. This chemical is likely to be found in specialized applications within the fields of organic synthesis, pharmaceuticals, or materials science, where its unique structure may confer specific chemical or biological activities.

79496-85-8

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79496-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79496-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,9 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79496-85:
(7*7)+(6*9)+(5*4)+(4*9)+(3*6)+(2*8)+(1*5)=198
198 % 10 = 8
So 79496-85-8 is a valid CAS Registry Number.

79496-85-8Downstream Products

79496-85-8Relevant academic research and scientific papers

Synthesis of Alkenyl Sulphoxides by Intramolecular and Intermolecular Addition of Sulphenic Acids to Alkynes

Bell, Richard,Cottam, Peter D.,Davies, John,Jones, D. Neville

, p. 2106 - 2115 (2007/10/02)

Alkyne-ω-sulphenic acids formed by thermolysis of ω-(t-butylsulphinyl)alkynes at 40 deg C cyclized regiospecifically to 2-methylenethiacycloalkane 1-oxides; 2-methylenethietan 1-oxide was not formed in this way. 2-Methylpropane-2-sulphenic acid, obtained by heating di-t-butyl sulphoxide, added regioselectively to oct-1-yne to give predominantly 2-t-butylsulphinyloct-1-ene, which itself decomposed thermally to a mixture of dioctenyl sulphoxides by way of alkenesulphenic acid-dialkyl sulphine interconversions.Benzenesulphenic acid, methanesulphenic acid, and ethoxycarbonylmethanesulphenic acid, conveniently generated by thermolysis of 1-cyano-2-alkyl(or aryl)sulphinylethanes, underwent intermolecular addition to unactivated and activated alkynes regioselectively to give alkenyl sulphoxides in good yields.

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