59276-12-9 Usage
Benzene ring
Aromatic ring with alternating single and double carbon-carbon bonds
Methoxy groups (-OCH3)
Two oxygen atoms bonded to a methyl group
Vinyl sulfide (-SCH3)
Sulfur atom bonded to a vinyl group (-CH=CH2) and a methyl group
Sulfoxide (-SOCH3)
Sulfur atom bonded to an oxygen atom and a methyl group
Structure
The molecule consists of a benzene ring with two methoxy groups attached to the 1st and 2nd carbon atoms, and a vinyl sulfide and sulfoxide group attached to the 3rd carbon atom.
Organic synthesis
Used as a versatile building block for creating more complex compounds
Pharmaceutical research
Potential applications in the development of pharmaceuticals
Agrochemicals
Potential use in the development of agrochemicals
Materials science
Potential applications in the development of new materials
Physical Properties
The specific physical properties (e.g., melting point, boiling point, solubility) are not provided in the material, but they can be inferred based on the molecular structure and functional groups.
Stability
The stability of the compound is not explicitly mentioned in the material, but the presence of multiple functional groups suggests that it may be sensitive to certain reaction conditions or reagents.
Check Digit Verification of cas no
The CAS Registry Mumber 59276-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59276-12:
(7*5)+(6*9)+(5*2)+(4*7)+(3*6)+(2*1)+(1*2)=149
149 % 10 = 9
So 59276-12-9 is a valid CAS Registry Number.
59276-12-9Relevant articles and documents
Acid Catalysed Reactions of Aryl Ketene Dithioacetal S-Oxides: Synthesis of Chloroketene Thioacetals and Thioesters
Hewson, Alan T.,Richardson, Stewart K.,Sharpe, David A.
, p. 2967 - 2970 (2007/10/02)
Aryl ketene dithioacetal S-oxides, on treatment with hydrochloric acid in dichloromethane, give chloroketene thioacetals.The same reaction in the presence of hydrogen sulphide gives S-methyl thioesters.
