244221-84-9 Usage
Description
(S)-(-)-1,2-Epithiooctane 90 is a chemical compound known for its strong sulfur-like odor, which is commonly found in garlic, onion, and other pungent foods, contributing to their characteristic aroma. It is also used as a flavoring agent in the food and beverage industry, a fragrance ingredient in perfumes and personal care products, and as a solvent in organic synthesis. The 90 designation may refer to the purity of the compound, indicating that it is 90% pure or a 90% solution in a specific solvent.
Uses
Used in Food and Beverage Industry:
(S)-(-)-1,2-Epithiooctane 90 is used as a flavoring agent for enhancing the aroma and taste of various food and beverage products, due to its strong, pungent odor.
Used in Perfume and Personal Care Products Industry:
(S)-(-)-1,2-Epithiooctane 90 is used as a fragrance ingredient in perfumes and personal care products, adding a unique and strong scent to these products.
Used in Chemical Production:
(S)-(-)-1,2-Epithiooctane 90 is used in the production of various chemical intermediates, playing a crucial role in the synthesis of different chemicals.
Used in Organic Synthesis:
(S)-(-)-1,2-Epithiooctane 90 is used as a solvent in organic synthesis, facilitating various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 244221-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,2 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 244221-84:
(8*2)+(7*4)+(6*4)+(5*2)+(4*2)+(3*1)+(2*8)+(1*4)=109
109 % 10 = 9
So 244221-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16S/c1-2-3-4-5-6-8-7-9-8/h8H,2-7H2,1H3/t8-/m0/s1
244221-84-9Relevant articles and documents
Catalytic Enantioselective Conversion of Epoxides to Thiiranes
Liao, Saihu,Leutzsch, Markus,Monaco, Mattia Riccardo,List, Benjamin
supporting information, p. 5230 - 5233 (2016/05/19)
A highly efficient and enantioselective Br?nsted acid catalyzed conversion of epoxides to thiiranes has been developed. The reaction proceeds in a kinetic resolution, furnishing both epoxide and thiirane in high yields and enantiomeric purity. Heterodimer formation between the catalyst and sulfur donor affords an effective way to prevent catalyst decomposition and enables catalyst loadings as low as 0.01 mol %.
