53475-18-6 Usage
Description
1-(methylsulfanyl)-1-phenylpropan-2-one, also known as thioacetone, is a chemical compound with the molecular formula C10H14OS. It is a colorless to pale yellow liquid with a strong, unpleasant odor. Thioacetone is commonly used as a reagent in organic synthesis and as a flavoring agent in the food industry. It is also a key intermediate in the production of pharmaceuticals, fragrances, and other chemical compounds. Thioacetone has the potential to be hazardous to human health and the environment, and it should be handled and stored with proper safety precautions.
Uses
Used in Organic Synthesis:
1-(methylsulfanyl)-1-phenylpropan-2-one is used as a reagent in organic synthesis for its ability to react with various compounds to form new chemical entities.
Used in Food Industry:
1-(methylsulfanyl)-1-phenylpropan-2-one is used as a flavoring agent in the food industry for its unique taste and aroma.
Used in Pharmaceutical Production:
1-(methylsulfanyl)-1-phenylpropan-2-one is used as a key intermediate in the production of pharmaceuticals for its role in the synthesis of various drug compounds.
Used in Fragrance Industry:
1-(methylsulfanyl)-1-phenylpropan-2-one is used as a key intermediate in the production of fragrances for its ability to contribute to the overall scent profile of various perfumes and scented products.
Used in Chemical Compounds Production:
1-(methylsulfanyl)-1-phenylpropan-2-one is used as a key intermediate in the production of other chemical compounds for its versatility in chemical reactions and its ability to form new compounds with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 53475-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,7 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53475-18:
(7*5)+(6*3)+(5*4)+(4*7)+(3*5)+(2*1)+(1*8)=126
126 % 10 = 6
So 53475-18-6 is a valid CAS Registry Number.
53475-18-6Relevant articles and documents
Syntheses of Arylacetone and Arylacetonitrile by Friedel-Crafts Reaction with α-Chloro-α-(methylthio)-substituted Acetone and Acetonitrile
Tamura, Yasumitsu,Choi, Hong Dae,Mizutani, Masako,Ueda, Yuko,Ishibashi, Hiroyuki
, p. 3574 - 3579 (2007/10/02)
Novel preparative methods for arylacetone and arylacetonitrile are described.Friedel-Crafts reactions of aromatic compounds with α-chloro-α-(methylthio)acetone (4) and α-chloro-α-(methylthio)acetonitrile (7) in the presence of Lewis acid afforded α-(methylthio)arylacetone (5) and α-(methylthio)arylacetonitrile (8), respectively.Compounds (5) and (8) were converted into the corresponding arylacetone (6) and arylacetonitrile (9) by reduction with zinc dust in acetic acid.Keywords: Friedel-Crafts reaction with α-chloro-α-(methylthio)acetone; Friedel-Crafts reaction with α-chloro-α-(methylthio)acetonitrile; α-(methylthio)arylacetone; α-(methylthio)arylacetonitrile; arylacetone; arylacetonitrile; reductive desulfurization; zinc dust-acetic acid
Introduction of α-(acyl) methylthiomethyl group into the aromatic ring by Friedel-Crafts reaction
Tamura,Shindo,Uenishi,Ishibashi
, p. 2547 - 2548 (2007/10/02)
Friedel-Crafts α-(acyl)methylthiomethylations of aromatic compounds with α-ethoxycarbonyl, -acetyl, -benzoyl, and -cyano-α-(methylthio)methyl chlorides are described. The resulted products are easily converted to acylmethylated aromatics such as phenylacetate and phenylacetone by reductive desulfurization.
