Molecular structure of 2-Chloro-2′,6′-diethylacetanilide, CAS Number: 6967-29-9
2-Chloro-2′,6′-diethylacetanilide (CAS 6967-29-9)
Alternate Names:
2-chloro-N-(2,6-diethylphenyl)acetamide
CAS Number:
6967-29-9
Molecular Weight:
225.71
Molecular Formula:
C12H16ClNO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2-Chloro-2′,6′-diethylacetanilide, also known as 2-Chloro-N-(2,6-diethylphenyl)acetamide, plays a role as an intermediate in the synthesis of numerous organic compounds and serves as a catalyst in diverse chemical reactions. Notably, this compound has demonstrated promising anti-cancer activity, as evidenced by its ability to impede the growth of various cancer cell lines. Moreover, 2-Chloro-2′,6′-diethylacetanilide has garnered attention in neurological disorder research due to its potential in reducing amyloid-β levels. Although the precise mechanism of action remains incompletely understood, it is believed to operate by inhibiting certain enzymes involved in glucose and fatty acid metabolism.
2-Chloro-2′,6′-diethylacetanilide (CAS 6967-29-9) References
- Hapten design in the development of competitive enyme-linked immunosorbent assays for genotoxic metabolites of alachlor. | Tessier, DM. and Clark, JM. 1999. J Agric Food Chem. 47: 3925-33. PMID: 10552745
- Leaching properties of some degradation products of alachlor and metolachlor. | Fava, L., et al. 2000. Chemosphere. 41: 1503-8. PMID: 11057589
- Determination of alachlor and two metabolites in groundwater using solid phase and a new micro-liquid-liquid extraction method | Heyer, R., Zapf, A., & Stan, H. J. 1995. Fresenius' journal of analytical chemistry. 351: 752-757.
- Rhizobacteria with Exceptionally High Aryl Acylamidase Activity | Hoagland, R. E., & Zablotowicz, R. M. 1995. Pesticide Biochemistry and Physiology. 52(3): 190-200.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Chloro-2′,6′-diethylacetanilide, 5 g | sc-265526 | 5 g | $84.00 |