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(1S,4S,9S,13S,16S)-4,8,8,16-Tetramethyltetracyclo<11.2.1.03,12.04,9>hexadecen-3(12)-ene is a complex organic compound characterized by its unique molecular structure. It features a tetracyclic ring system with a hexadecen-3(12)-ene backbone, indicating the presence of a 16-carbon chain with a double bond between carbons 3 and 12. The compound is further defined by four methyl groups attached at specific positions, which are crucial for its stereochemistry. The stereochemistry is denoted by the prefixes (1S,4S,9S,13S,16S), indicating that the chiral centers at these positions have the S configuration. (1S,4S,9S,13S,16S)-4,8,8,16-Tetramethyltetracyclo<11.2.1.03,12.04,9>hexadecen-3(12)-ene is likely to be found in specialized chemical research or pharmaceutical applications due to its intricate structure and potential for specific interactions in biological systems.

31908-68-6

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31908-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31908-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,0 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31908-68:
(7*3)+(6*1)+(5*9)+(4*0)+(3*8)+(2*6)+(1*8)=116
116 % 10 = 6
So 31908-68-6 is a valid CAS Registry Number.

31908-68-6Downstream Products

31908-68-6Relevant academic research and scientific papers

SUPERACID ISOMERIZATION OF PHYLLOCLADENE, ISOPHYLLOCLADENE, AND PHYLLOCLADANOL

Vlad, P. F.,Ungur, N. D.,Barba, A. N.,Tatarova, L. E.,Gatilov, Yu. V.,et al.

, p. 301 - 308 (2007/10/02)

It has been established that, on interaction with a superacid, phyllocladene (XI), isophyllocladene (XV), and phyllocladan-16-ol (XIX) give identical mixtures of substances which include phyllocladene (XI), isophyllocladene (XV), neoisoatisene (XX), tetracyclic hydrocarbons with a new carbon skeleton (XXI) and (XXII), and a mixture of methyl ethers of alcohols formed as the result of the addition of methanol to the carbocations arising on the protonation of the above-mentioned hydrocarbons.

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