49833-33-2 Usage
Description
Propanoic acid, 3-[(1,1-dimethylethyl)thio]-, ethyl ester is a chemical compound that is commonly used as a flavoring agent in food and beverages. It is also used in the production of fragrances and as a solvent in various industries. Propanoic acid, 3-[(1,1-dimethylethyl)thio]-, ethyl ester is a clear, colorless liquid with a fruity odor and is flammable. It is important to handle this chemical with care as it can be harmful if ingested, inhaled, or comes into contact with the skin and eyes. Additionally, it may pose a risk to the environment if not properly disposed of.
Uses
Used in Food and Beverage Industry:
Propanoic acid, 3-[(1,1-dimethylethyl)thio]-, ethyl ester is used as a flavoring agent to enhance the taste and aroma of various food and beverage products.
Used in Fragrance Industry:
Propanoic acid, 3-[(1,1-dimethylethyl)thio]-, ethyl ester is used in the production of fragrances to provide a fruity scent to various products.
Used in Various Industries as a Solvent:
Propanoic acid, 3-[(1,1-dimethylethyl)thio]-, ethyl ester is used as a solvent in various industries due to its ability to dissolve other substances and its flammable nature.
Check Digit Verification of cas no
The CAS Registry Mumber 49833-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,3 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 49833-33:
(7*4)+(6*9)+(5*8)+(4*3)+(3*3)+(2*3)+(1*3)=152
152 % 10 = 2
So 49833-33-2 is a valid CAS Registry Number.
49833-33-2Relevant articles and documents
Sulfenate substitution as a complement and alternative to sulfoxidation in the diastereoselective preparation of chiral β-substituted β-amino sulfoxides
S?derman, Stefan C.,Schwan, Adrian L.
, p. 1638 - 1649 (2013/03/28)
Building from a previous communication, the reaction of sulfenate anions with chiral N-Boc-protected β-substituted β-amino iodides was evaluated as a conceptually different synthetic approach to chiral β-substituted β-amino sulfoxides. Using arenesulfenat
Synthetic Uses of Thio- and Selenoesters of Trifluoromethylated Acids. 1. Preparation of Trifluoromethyl Sulfides and Selenides
Billard, Thierry,Roques, Nicolas,Langlois, Bernard R.
, p. 3813 - 3820 (2007/10/03)
Trifluorothioacetates (CF3CO-S-R, from (CF3CO)2O and thiols) as well as trifluoromethanethio-or trifluoromethaneselenosulfonates (CF3SO2-Y-R; Y = S, Se; from CF3SO2Na, RYYR, and Br2) can be formally decarbonylated or desulfonylated, respectively, provided that they are photolyzed at 40°C in the presence of 1 equiv of the corresponding disulfide or diselenide. Trifluoromethyl sulfides or selenides are obtained, and the added disulfide (or diselenide) is recovered after reaction. In such a way, S-(trifluoromethyl)cysteine derivatives can be obtained.
