38634-59-2 Usage
Uses
Used in Flavoring Industry:
(Methylthio)methylthiolacetate is used as a flavoring agent for its pungent and sulfurous aroma, enhancing the taste and smell of food and beverages.
Used in Cosmetics Production:
In the cosmetics industry, (Methylthio)methylthiolacetate is used as a component in the production of various products, capitalizing on its distinctive odor to create appealing scents.
Used in Fragrance Industry:
(Methylthio)methylthiolacetate is also utilized in the fragrance industry to add a unique and strong onion-like scent to different perfumes and scented products.
Used in Consumer Products:
(Methylthio)methylthiolacetate is employed in the production of other consumer products, such as cleaning agents and air fresheners, to provide a characteristic smell.
Safety Precautions:
It is crucial to handle (Methylthio)methylthiolacetate with care, as it can cause skin and eye irritation. It is recommended to use (Methylthio)methylthiolacetate in well-ventilated areas to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 38634-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,3 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38634-59:
(7*3)+(6*8)+(5*6)+(4*3)+(3*4)+(2*5)+(1*9)=142
142 % 10 = 2
So 38634-59-2 is a valid CAS Registry Number.
38634-59-2Relevant academic research and scientific papers
Mechanism in the chlorinolysis of sulfinyl chlorides
Ahern, Terence Patrick,Haley, Michael Francis,Langler, Richard Francis,Trenholm, June Ellen
, p. 610 - 614 (2007/10/02)
The successful synthesis and chlorinolysis of α-mercaptodimethyl sulfone have provided additional support for our contention that Pummerer rearrangements may occur during the chlorinolyses of α-sulfonyl sulfinyl chlorides.Further exploration of chlorinolyses of α-sulfonyl systems has uncovered the first observation of CS bond cleavage during the chlorinolyses of (i) a sulfinyl chloride and (ii) a sulfinate ester.
