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1-(allylsulfinyl)-2-nitrobenzene is an organic compound characterized by a benzene ring with a nitro group at the 2-position and an allyl sulfinyl group at the 1-position. The allyl sulfinyl group consists of a sulfur atom bonded to an allyl group (CH2=CH-CH2) and an oxygen atom. 1-(allylsulfinyl)-2-nitrobenzene is known for its unique chemical properties, which include reactivity towards nucleophiles due to the electron-withdrawing effect of the nitro group and the presence of a sulfinyl group, which can act as a chiral center. It is often used in organic synthesis as a building block for more complex molecules, particularly in the preparation of pharmaceuticals and agrochemicals. The compound's structure and reactivity make it a valuable intermediate in the synthesis of various biologically active compounds.

1659-00-3

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1659-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1659-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1659-00:
(6*1)+(5*6)+(4*5)+(3*9)+(2*0)+(1*0)=83
83 % 10 = 3
So 1659-00-3 is a valid CAS Registry Number.

1659-00-3Relevant academic research and scientific papers

Dynamic kinetic resolution of allylic sulfoxides by Rh-catalyzed hydrogenation: A combined theoretical and experimental mechanistic study

Dornan, Peter K.,Kou, Kevin G. M.,Houk,Dong, Vy M.

supporting information, p. 291 - 298 (2014/01/23)

A dynamic kinetic resolution (DKR) of allylic sulfoxides has been demonstrated by combining the Mislow [2,3]-sigmatropic rearrangement with catalytic asymmetric hydrogenation. The efficiency of our DKR was optimized by using low pressures of hydrogen gas to decrease the rate of hydrogenation relative to the rate of sigmatropic rearrangement. Kinetic studies reveal that the rhodium complex acts as a dual-role catalyst and accelerates the substrate racemization while catalyzing olefin hydrogenation. Scrambling experiments and theoretical modeling support a novel mode of sulfoxide racemization which occurs via a rhodium π-allyl intermediate in polar solvents. In nonpolar solvents, however, the substrate racemization is primarily uncatalyzed. Computational studies suggest that the sulfoxide binds to rhodium via O-coordination throughout the catalytic cycle for hydrogenation.

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