85939-98-6 Usage
Description
Methyl 3-(Methoxysulfinyl)propanoate is an organic compound characterized by the chemical formula C6H12O4S. It is recognized for its distinctive fruity and nutty aroma, which makes it a popular choice as a flavoring agent and food additive. Methyl 3-(Methoxysulfinyl)propanoate also finds applications in the production of pharmaceuticals, insecticides, and fragrances. Its stability and non-reactivity under normal conditions contribute to its suitability for a diverse range of uses. However, it is crucial to handle Methyl 3-(Methoxysulfinyl)propanoate with care and adhere to safety protocols when working with it.
Uses
Used in Flavor and Fragrance Industry:
Methyl 3-(Methoxysulfinyl)propanoate is used as a flavoring agent for its fruity and nutty aroma, enhancing the taste and smell of various food products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Methyl 3-(Methoxysulfinyl)propanoate is utilized in the production of drugs, capitalizing on its chemical properties to contribute to the development of medicinal formulations.
Used in Agriculture:
Methyl 3-(Methoxysulfinyl)propanoate is employed in the creation of insecticides, where its chemical composition plays a role in controlling or repelling pests.
Used in Cosmetics and Personal Care Industry:
Methyl 3-(Methoxysulfinyl)propanoate is also used in fragrances for cosmetics and personal care products, providing a pleasant scent and enhancing the sensory experience of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 85939-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,3 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85939-98:
(7*8)+(6*5)+(5*9)+(4*3)+(3*9)+(2*9)+(1*8)=196
196 % 10 = 6
So 85939-98-6 is a valid CAS Registry Number.
85939-98-6Relevant articles and documents
Direct synthesis of sulfinic esters via ultrasound accelerated tandem reaction of thiols and alcohols with N-bromosuccinimide
Nguyen, Lan-Anh Thi,Le, Tri-Nghia,Duong, Cong-Thang,Vo, Chi-Tam,Duus, Fritz,Luu, Thi Xuan Thi
, p. 519 - 528 (2021/05/27)
The direct transformation of various thiols and simple alcohols with N-bromosuccinimide into sulfinic esters has been investigated by using different categories of base/acidic catalysts as well as co-solvents under varied reaction conditions. The reaction was found out to afford the sulfinic esters with high yields in the absence of catalysts, especially within the shorter time under the acceleration of ultrasonic irradiation than under the longer-lasting conventional stirring conditions.
SULFINIC ACIDS AND RELATED COMPOUNDS. 15. CONVENIENT METHODS FOR ESTERIFYING SENSITIVE SULFINIC ACID SALTS
Srivastava, Pramod K.,Field, Lamar
, p. 161 - 166 (2007/10/02)
In a study of conversions of sensitive sulfinate salts to esters, a trisulfide bissulfinate, 2S (1), was esterified with trialkyloxonium fluorborates.This procedure (Method A) was better for ethylation than use of ROH-HCl/BF3*(C2H5)2O (Metho
