| Identification | Back Directory | [Name]
N-[[(Z)-but-2-enoxy]methyl]-2-chloro-N-(2,6-diethylphenyl)acetamide | [CAS]
87310-56-3 | [Synonyms]
Kh-218
butenachlor
(Z)-N-But-2-enyloxymethyl-2-chloro-2',6'-diethylacetanilide (iupac)
N-[[(Z)-but-2-enoxy]methyl]-2-chloro-N-(2,6-diethylphenyl)acetamide
(Z)-N-(2,6-Diethylphenyl)-N-((2-butenyloxy)methyl)-2-chloroacetamide
Acetamide, N-(2,6-diethylphenyl)-N-((2-butenyloxy)methyl)-2-chloro-, (Z)-
Acetamide, N-[[(2Z)-2-buten-1-yloxy]methyl]-2-chloro-N-(2,6-diethylphenyl)- | [Molecular Formula]
C17H24ClNO2 | [MDL Number]
MFCD01670496 | [MOL File]
87310-56-3.mol | [Molecular Weight]
309.83 |
| Chemical Properties | Back Directory | [Boiling point ]
442.3±45.0 °C(Predicted) | [density ]
1.090±0.06 g/cm3(Predicted) | [pka]
1.18±0.50(Predicted) | [Henry's Law Constant]
1.0×102 mol/(m3Pa) at 25℃, MacBean (2012) |
| Hazard Information | Back Directory | [Description]
Butenachlor is a soil-applied herbicide. It has a moderate aqueous solubility and is not highly volatile. It is not expected to be persistent in soil systems. It is moderately toxic to fish but less so to birds. It has a low mammalian oral toxicity. | [Uses]
Butenachlor is a herbicide. | [Production Methods]
Butenachlor is produced commercially through a sequence of reactions typical for this class of compounds. The process begins with the synthesis of the substituted aniline precursor, which is then reacted with chloroacetyl chloride under controlled conditions to form the chloroacetanilide backbone. Subsequent alkylation introduces the butoxyethyl side chain, yielding the active butenachlor molecule. | [Mechanism of action]
Inhibits cell division by blocking protein synthesis | [Pesticide Type]
Herbicide |
|
|