33922-73-5 Usage
Description
2-PROPENYL PROPYL TRISULFIDE is an organic compound that is derived from the combination of allyl and propyl groups with a trisulfide bridge. It is known for its unique chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
2-PROPENYL PROPYL TRISULFIDE is used as an additive for garlic oil to enhance the bioavailability of coenzyme-10. This application is particularly relevant in the pharmaceutical industry, where improving the absorption and effectiveness of essential nutrients and supplements is crucial for overall health and well-being.
Application Reason:
The use of 2-PROPENYL PROPYL TRISULFIDE in the pharmaceutical industry is primarily due to its ability to increase the bioavailability of coenzyme-10 when used alongside garlic oil. This enhancement in bioavailability can lead to improved health outcomes and more effective treatment options for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 33922-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,2 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33922-73:
(7*3)+(6*3)+(5*9)+(4*2)+(3*2)+(2*7)+(1*3)=115
115 % 10 = 5
So 33922-73-5 is a valid CAS Registry Number.
33922-73-5Relevant articles and documents
Unsymmetrical Organotrisulfide Formation via Low-Temperature Disulfanyl Anion Transfer to an Organothiosulfonate
Ali, Doaa,Hunter, Roger,De Doncker, Stephen,Rees-Jones, Sophie C. M.,Kaschula, Catherine H.
, p. 2862 - 2869 (2019/03/23)
New methodology is presented for the formation of unsymmetrical organotrisulfides in a high yield and purity, relatively free of polysulfide byproducts. The highlight of the method is the low-temperature (-78 °C) deprotection of a disulfanyl acetate with sodium methoxide in THF to form a disulfanyl anion, which reacts rapidly in situ with an organothiosulfonate (S-aryl or S-alkyl) within 30 seconds followed by quenching. The discovery of these new reaction conditions together with the relative greenness of the chemistry overall makes for an efficient protocol, from which a range of organotrisulfides covering aliphatic, aromatic, as well as cysteine and sugar groups can be accessed in a high yield and purity.