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(R/S)-3-(p-tolylthio)isobenzofuran-1(3H)-one is a chiral organic compound characterized by its unique structure and properties. It features a 3H-isobenzofuran-1-one core, which is a heterocyclic aromatic ring system, with a p-tolylthio group (a tolyl group attached to a sulfur atom) at the 3-position. The compound exists as a pair of enantiomers due to the presence of a chiral center, indicated by the (R/S) notation. This chirality can significantly influence the compound's reactivity and biological activity. The compound may have potential applications in the synthesis of pharmaceuticals or other organic compounds, as well as in the study of chiral chemistry.

53912-20-2

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53912-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53912-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53912-20:
(7*5)+(6*3)+(5*9)+(4*1)+(3*2)+(2*2)+(1*0)=112
112 % 10 = 2
So 53912-20-2 is a valid CAS Registry Number.

53912-20-2Relevant academic research and scientific papers

TiCl 4 -Mediated Synthesis of 3,4-Hetero-Disubstituted Isocoumarins by Means of Isocyanide Insertion Reactions

Ponra, Sudipta,Nyadanu, Aude,Maurin, Sylvie,El Ka?m, Laurent,Grimaud, Laurence,Vitale, Maxime R.

, p. 1331 - 1342 (2017/12/26)

The isocyanide insertion into sulfanyl-phthalides under Lewis acid conditions is reported with full details. This sequential three-component reaction affords a new straightforward and highly convenient method for the preparation of 3-amino-4-sulfanyl isocoumarins, the potential of which is still unexplored.

Hauser–Kraus Annulation of Phthalides with Nitroalkenes for the Synthesis of Fused and Spiro Heterocycles

Kumar, Tarun,Satam, Nishikant,Namboothiri, Irishi N. N.

supporting information, p. 3316 - 3321 (2016/07/26)

Hauser–Kraus annulation of sulfonylphthalides with simple conjugated nitroalkenes follows the expected pathway to furnish naphthoquinones in moderate yields. However, a strategic variation of this reaction by employing nitroalkenes bearing an additional nucleophilic site results in [4+4] annulation leading to complex fused and spiro heterocycles in high yields with high selectivity through a cascade process involving Michael addition, Dieckmann cyclization, and a series of eliminations and rearrangements.

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