5391-78-6 Usage
Uses
Used in Flavor and Fragrance Industry:
1,7,7-Trimethylnorbornane-2-thiol is utilized as a flavor and fragrance ingredient, providing a unique sulfurous and thiol-like aroma to a variety of products. Its distinctive scent profile makes it a valuable addition in the creation of complex and nuanced fragrances and flavors.
Used in Organic Chemistry:
As a reagent in organic chemistry, 1,7,7-trimethylnorbornane-2-thiol is employed in the synthesis of other thiol-containing compounds. Its reactivity and sulfur-containing structure make it a key component in various chemical reactions, contributing to the development of new organic compounds.
Used in Pharmaceutical Development:
1,7,7-Trimethylnorbornane-2-thiol is studied for its potential applications in the pharmaceutical industry. Its unique chemical properties and reactivity may offer new avenues for the development of therapeutic agents, particularly in the synthesis of novel drug candidates.
Used in Agrochemical Development:
Similarly, this compound is being explored for its potential in agrochemical development. Its properties may contribute to the creation of new agrochemicals, enhancing crop protection and management strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 5391-78-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5391-78:
(6*5)+(5*3)+(4*9)+(3*1)+(2*7)+(1*8)=106
106 % 10 = 6
So 5391-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H18S/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3
5391-78-6Relevant 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.
