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α-(Trimethylsilylethinylthiomethyl)zimtsaeurenitril is a complex organic compound with the chemical formula C9H18N2SSi. It is characterized by the presence of a trimethylsilyl group (Si(CH3)3), a thioether linkage (S), and a nitrile group (C≡N). α-(Trimethylsilylethinylthiomethyl)zimtsaeurenitril is a derivative of zimtsaeurenitril, which is a type of nitriles that can be found in certain natural products. The trimethylsilylethinylthiomethyl group adds a unique structural feature to the molecule, potentially affecting its reactivity and properties. Such compounds are often studied for their synthetic potential and applications in various chemical processes, including the formation of new bonds and the modification of existing ones.

86318-46-9

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86318-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86318-46-9 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, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86318-46:
(7*8)+(6*6)+(5*3)+(4*1)+(3*8)+(2*4)+(1*6)=149
149 % 10 = 9
So 86318-46-9 is a valid CAS Registry Number.

86318-46-9Relevant 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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