N-(2-butoxyethyl)-2-chloroacetamide
Names and Identifiers of N-(2-butoxyethyl)-2-chloroacetamide
CAS Number |
1193387-64-2 |
|---|---|
IUPAC Name |
N-(2-butoxyethyl)-2-chloroacetamide |
InChI |
InChI=1S/C8H16ClNO2/c1-2-3-5-12-6-4-10-8(11)7-9/h2-7H2,1H3,(H,10,11) |
InChIKey |
PUFYPMPHTLDFEF-UHFFFAOYSA-N |
Canonical SMILES |
CCCCOCCNC(=O)CCl |
Physical and chemical properties of N-(2-butoxyethyl)-2-chloroacetamide
Acidity coefficient |
13.62±0.46(Predicted) |
|---|---|
Boiling Point |
322.2±27.0 °C(Predicted) |
Density |
1.050±0.06 g/cm3(Predicted) |
Molecular Formula |
C8H16ClNO2 |
Molecular Weight |
193.67 |
Safety Information of N-(2-butoxyethyl)-2-chloroacetamide
Applications of N-(2-butoxyethyl)-2-chloroacetamide
N-(2-butoxyethyl)-2-chloroacetamide finds applications primarily in:
- Agricultural Chemistry: Used as an herbicide due to its effectiveness in controlling unwanted vegetation.
- Biochemical Research: Employed in proteomics studies for its ability to modify proteins and peptides.
- Pharmaceutical Development: Potentially useful in developing new therapeutic agents due to its biological activity.
Interaction Studies of N-(2-butoxyethyl)-2-chloroacetamide
Studies on N-(2-butoxyethyl)-2-chloroacetamide interactions focus on its behavior in biological systems and its reactivity with various nucleophiles. It has been noted that the compound may interact with cellular components, influencing metabolic pathways and potentially leading to cytotoxic effects in certain conditions. Further research is needed to fully elucidate these interactions and their implications for both safety and efficacy in agricultural use.
Biological Activity of N-(2-butoxyethyl)-2-chloroacetamide
The biological activity of N-(2-butoxyethyl)-2-chloroacetamide has been explored primarily in the context of its herbicidal properties. Chloroacetamides are known to inhibit the growth of various weeds by interfering with their seed germination and root development. This compound may also exhibit cytotoxic effects against certain cell lines, making it a candidate for further pharmacological studies.