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α-(tert-Butylthioethinylthiomethyl)zimtsaeure-methylester is a complex organic compound with the chemical formula C15H22O2S3. It is a derivative of α-(thioalkylthiomethyl)zimtsaeure-methylester, which is a class of compounds known for their potential applications in various chemical and pharmaceutical processes. This specific compound features a methyl ester group attached to a zingerone backbone, which is a phenolic compound derived from ginger. The tert-butylthioethinylthiomethyl group adds to its complexity, providing unique chemical properties. While the exact applications of α-(tert-Butylthioethinylthiomethyl)zimtsaeure-methylester are not widely documented, it is likely to be used in research settings or as an intermediate in the synthesis of more complex molecules. Due to its specialized nature, it is not a common household or industrial chemical but rather a substance of interest to chemists and researchers in the field of organic synthesis.

86318-59-4

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86318-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86318-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,1 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86318-59:
(7*8)+(6*6)+(5*3)+(4*1)+(3*8)+(2*5)+(1*9)=154
154 % 10 = 4
So 86318-59-4 is a valid CAS Registry Number.

86318-59-4Relevant academic research and scientific papers

Thioketene Syntheses, VII. Substituent Effects on the Thio-Claisen Rearrangement of Alkynyl Allyl Sulfides

Schaumann, Ernst,Lindstaedt, Joerg

, p. 1728 - 1738 (2007/10/02)

Electron acceptors in the position 2 of the allyl residues in alkynyl allyl sulfides 4, 11, 15 favor the Thio-Claisen rearrangement to give thioketenes 5, 12, 16, but in position 3 impede the reaction.For the substituent on the triple bond, the sequence silyl > alkyl > alkylthio is valid.The results can be understood in terms of a zwitterionic intermediate 19 or a highly polarized transition state of the rearrangement.

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