5952-75-0 Usage
Uses
Used in Flavoring Agents:
2-methyl-4-(methylsulfanyl)but-1-ene is utilized as a flavoring agent in the food industry, where its unique and pungent odor contributes to the enhancement of various food products' aroma and taste. Its application in this industry is primarily due to its ability to impart a distinct flavor profile to the products, making them more appealing to consumers.
Used in Chemical Synthesis:
In the chemical industry, 2-methyl-4-(methylsulfanyl)but-1-ene may also serve as a starting material or intermediate in the synthesis of other organic compounds. Its chemical reactivity, stemming from the presence of the butene backbone and the methylsulfanyl group, allows it to participate in various chemical reactions, leading to the formation of a wide range of products with diverse applications.
Used in Fragrance Industry:
2-methyl-4-(methylsulfanyl)but-1-ene is employed as a component in the creation of fragrances and perfumes. Its strong and distinctive odor makes it a valuable addition to the formulation of various scented products, such as perfumes, colognes, and other personal care items. Its use in this industry is driven by its ability to provide a unique and long-lasting scent that can be appreciated by consumers.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 2-methyl-4-(methylsulfanyl)but-1-ene may also find applications in the pharmaceutical industry. Given its chemical structure and reactivity, it could potentially be used as a building block for the synthesis of various pharmaceutical compounds or as a component in drug formulations, depending on its bioactivity and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 5952-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5952-75:
(6*5)+(5*9)+(4*5)+(3*2)+(2*7)+(1*5)=120
120 % 10 = 0
So 5952-75-0 is a valid CAS Registry Number.
5952-75-0Relevant academic research and scientific papers
The regiochemistry of cyclization of α-sulfenyl-, α-sulfinyl-, and α-sulfonyl-5-hexenyl radicals: Procedures leading to regioselective syntheses of cyclic sulfones and sulfoxides
Della, Ernest W.,Graney, Sean D.
, p. 3824 - 3835 (2007/10/03)
A study of the cyclization of α-sulfenyl-, α-sulfinyl-, and α-sulfonyl-5-hexenyl and 5-methyl-5-hexenyl radicals reveals a unique contrast in the mode of ring closure of the radicals. In the case of the 5-hexenyl radicals, the sulfinyl-substituted species displays unexpected regioselectivity relative to its analogues. Thus, while the α-S- and α-SO2-5-hexenyl radicals give measurable and increasing quantities of 6-endo product, the α-sulfinyl species cyclizes with high selectivity (95.5:4.5) via a 5-exo mode. By contrast, ring closure of the 5-methyl-5-hexenyl radicals is found to give substantially the 6-endo product in all cases. It is the α-sulfonyl-5-methyl-5-hexenyl radical that now exhibits high regioselectivity (97.5:2.5) for 6-endo closure: an illustration of the synthetic value of this observation is the independent synthesis of the model cyclohexyl sulfone 61 in high yield. It is found that ring closure under the conditions employed occurs irreversibly in all cases.
Regioselectivity of ring closure of 2-thia- and 2-sulfonyl-5-methyl-5-hexenyl radicals
Della, Ernest W.,Graney, Sean D.
, p. 4065 - 4067 (2007/10/03)
(matrix presented) Ring closure of the α-substituted radicals 4 (X = S, SO2) is observed to be irreversible and to lead to significant amounts of the product of 6-endo cyclization. Indeed, reduction of the sulfonyl-based radical 4 (X = SO2
