52195-40-1 Usage
Description
(Z)-2-Thia-3-pentene, also known as Z-1-Methylthio-1-propene, is an organic compound characterized by the presence of a sulfur atom and a double bond in its structure. It is a volatile organic compound that can be found among the components of various natural sources, such as onions. Due to its unique chemical properties, it has potential applications in different fields, particularly in the study of structure-stability relationships in unsaturated sulfur compounds.
Uses
Used in Chemical Research:
(Z)-2-Thia-3-pentene is used as a research compound for studying the structure-stability relationships in unsaturated sulfur compounds. Its unique structure allows scientists to gain insights into the behavior and properties of similar compounds, which can be beneficial for the development of new materials and chemicals.
Used in Flavor and Fragrance Industry:
As one of the volatile organic components of onion, (Z)-2-Thia-3-pentene is used as a flavoring agent and additive in the food and beverage industry. Its characteristic aroma can be utilized to enhance the taste and smell of various products, contributing to a more enjoyable consumer experience.
Used in Pharmaceutical Industry:
(Z)-2-Thia-3-pentene may also have potential applications in the pharmaceutical industry, particularly in the development of new drugs targeting sulfur-containing enzymes or proteins. Its unique chemical structure can be exploited to design novel therapeutic agents with specific interactions and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 52195-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,9 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52195-40:
(7*5)+(6*2)+(5*1)+(4*9)+(3*5)+(2*4)+(1*0)=111
111 % 10 = 1
So 52195-40-1 is a valid CAS Registry Number.
52195-40-1Relevant articles and documents
Isomerization processes in the synthesis of asymmetric allyl chalcogenides
Deryagina,Korchevin
, p. 223 - 225 (1996)
Allyl-propenyl rearrangement (prototropic isomerization) occurs in the synthesis of allyl organyl chalcogenides in a hydrazine hydrate - KOH system with a 6 - 10-fold molar excess of KOH. Specificities of the rearrangement that depend on the nature of the chalcogen were studied.
