61366-76-5 Usage
Uses
Used in Flavor Industry:
Methyl 2-methylthiopropionate is used as a flavoring agent for imparting the true note of pineapple to various products. Its ability to contribute to the overall aroma perception of ripe fruit makes it a valuable addition to the flavor industry.
Used in Beverages:
Methyl 2-methylthiopropionate is used as a flavor enhancer in the beverage industry, particularly for products that aim to capture the essence of pineapple flavor. It is added at a concentration of 0.5–1 ppm to provide a subtle and authentic taste.
Used in Ice Cream:
In the ice cream industry, Methyl 2-methylthiopropionate is utilized as a flavoring agent to create pineapple-flavored ice cream. Its unique fruity odor with a hint of sulfur helps to deliver a more natural and enjoyable pineapple taste.
Used in Candy:
Methyl 2-methylthiopropionate is employed in the candy industry to add a distinct pineapple flavor to various confections. Its use at 0.5–1 ppm ensures that the candy maintains a true and pleasant pineapple aroma.
Used in Baked Goods:
In the baked goods industry, Methyl 2-methylthiopropionate is used as a flavoring agent to enhance the taste of pineapple-flavored baked products. Its addition at the specified concentration allows for a more authentic and enjoyable pineapple experience in baked goods.
Check Digit Verification of cas no
The CAS Registry Mumber 61366-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61366-76:
(7*6)+(6*1)+(5*3)+(4*6)+(3*6)+(2*7)+(1*6)=125
125 % 10 = 5
So 61366-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O2S/c1-4(8-3)5(6)7-2/h4H,1-3H3
61366-76-5Relevant academic research and scientific papers
MgBr2-Promoted Addition of Heterosubstituted Methylketene Silyl Acetals to Alkoxy Aldehydes. Diastereoselective Synthesis of 3,4-Syn 2-Methylene- and 2-(Alkoxymethyl)-3-hydroxy-4-alkoxy Esters
Bernardi, Anna,Cardani, Silvia,Colombo, Lino,Poli, Giovanni,Schimperna, Giuliana,Scolastico, Carlo
, p. 888 - 891 (2007/10/02)
The MgBr2-mediated addition of 2- or 3-(methylthio)-substituted ketene silyl acetals 3 and 4 to α-alkoxy and α,β-dialkoxy aldehydes, followed by oxidation and elimination of methanesulfenic acid, gave 3,4-syn 2-methylene-3-hydroxy-4-alkoxy esters 9 and 11 with very high stereoselectivity (up to 100:1) and in good chemical yields.The same diastereofacial selection is at work in the analogous additions of ketene methyl silyl acetal 5, which affords 3,4-syn 2--3-hydroxy-4-alkoxy esters 12-15.
