68134-79-2 Usage
General Description
1,8-Dihydroxy-2,8-dithiocyclotetradecane is a chemical compound that is also known as thiolutin. It is a natural product isolated from the bacterium Streptomyces sp. 1,8-Dihydroxy-2,8-dithiocyclotetradecane has demonstrated potential anti-tumor and anti-inflammatory properties in various studies. It has also been found to inhibit the growth of several types of cancer cells, making it a promising candidate for further research and potential drug development. Additionally, it has shown the ability to inhibit the production of inflammatory cytokines, indicating its potential for use in treating inflammatory conditions. Overall, 1,8-Dihydroxy-2,8-dithiocyclotetradecane appears to have a range of bioactive properties that warrant further investigation for potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 68134-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,3 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68134-79:
(7*6)+(6*8)+(5*1)+(4*3)+(3*4)+(2*7)+(1*9)=142
142 % 10 = 2
So 68134-79-2 is a valid CAS Registry Number.
InChI:InChI=1S/C12H20O2S2/c13-11-7-3-1-5-9(11)15-12(14)8-4-2-6-10(12)16-11/h9-10,13-14H,1-8H2
68134-79-2Relevant articles and documents
The Willgerodt-Kindler Reactions. 6. Isomerization of the Carbonyl Group in Alkanones and Cycloalkanones
Carmack, Marvin,Behforouz, Mohammad,Berchtold, Glenn A.,Berkowitz, Samuel M.,Wiesler, Donald,Barone, Ralph
, p. 1305 - 1318 (2007/10/02)
The most unusual feature of the Willgerodt-Kindler Reactions is the facile isomerization of the carbonyl function along a chain of unbranched methylene groups, or around a cycloaliphatic ring containing several connected methylene groups.We have demonstrated that the first step in the Kindler process is the formation of enamines by reaction of the carbonyl function with secondary aliphatic amines, followed by reaction of the enamine with certain sulfur-amine catalysts to form reactive heterocyclic sulfur intermediates that facilitate the elimination-readdition of the amines reversibly along the chain.It was shown that compounds of the type R2N-S-S-NR2 are effective catalysts but not compounds of the type R2N-S-NR2.Some cyclohexanone derivatives undergo aromatization, with anomalous results in certain cases.
