4-(2-(2-bromophenoxy)ethyl)thiomorpholine
$300.00
CAS No.: 1823235-00-2
Catalog No.: 197697
Purity: 95%
MF: C12H16BrNOS
MW: 302.237
Storage: 2-8 degree Celsius
SMILES: BrC1=C(OCCN2CCSCC2)C=CC=C1
Catalog No.: 197697
Purity: 95%
MF: C12H16BrNOS
MW: 302.237
Storage: 2-8 degree Celsius
SMILES: BrC1=C(OCCN2CCSCC2)C=CC=C1
4-(2-(2-bromophenoxy)ethyl)thiomorpholine; CAS No.: 1823235-00-2;4-(2-(2-bromophenoxy)ethyl)thiomorpholine. PROPERTIES: 4-(2-(2-bromophenoxy)ethyl)thiomorpholine is a substituted thiomorpholine with a molecular weight of 305.21 g/mol. This colorless liquid has a boiling point around 185-187 C at 760 mmHg. The molecule features a thiomorpholine ring substituted at position 4 with a 2-(2-bromophenoxy)ethyl group. It demonstrates moderate solubility in common organic solvents such as ethanol and acetone and limited water solubility. Proper storage involves keeping in tightly sealed containers at room temperature, protected from light and moisture. Safety considerations include the bromine substituent's potential to cause skin irritation and the thiomorpholine ring's general toxicity. Proper protective equipment should be utilized during handling. APPLICATIONS: This compound primarily serves as a synthetic intermediate in the production of agrochemicals and pharmaceuticals, where the brominated phenoxy substituent provides versatile sites for cross-coupling reactions. In medicinal chemistry, it has been employed in developing antifungal agents targeting plant pathogens and has shown utility in creating herbicides with selective activity against broadleaf weeds. The thiomorpholine-phenoxy structure has also been explored in materials science for developing chiral ligands in asymmetric catalysis, leveraging the sulfur atom's stereoelectronic effects. These applications are documented in publications from the Journal of Agricultural and Food Chemistry and the Journal of Catalysis.
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