| Identification | Back Directory | [Name]
3',4'-DICHLOROCYCLOPROPANECARBOXANILIDE | [CAS]
2759-71-9 | [Synonyms]
S-6000
Clobber
Cipromid
Cypromid
Cypronid
Cypromide
s-6000[qr]
cipromid[qr]
trans-4-(2-Chlorocyclopropyl)anisol
TRANS-4-(2-CHLOROCYCLOPROPYL) ANISOLE
3’,4’-dichloro-cyclopropanecarboxanilid
3',4'-DICHLOROCYCLOPROPANECARBOXANILIDE
cyclopropanecarboxanilide,3’,4’-dichloro-
3’,4’-dichlorocyclopropanecarboxanilide[qr]
n-(3,4-dichlorophenyl)-cyclopropanecarboxamid
N-(3,4-Dichlorophenyl)cyclopropanecarboxamide
N-(3,4-Dichlorophenyl)cyclopropanecarboxyamide
3,4-dichloranilidkyselinycyklopropankarboxylove
N-(3,4-Dichlorophenyl)cyclopropane-1-carboxamide
Cyclopropanecarboxamide, N-(3,4-dichlorophenyl)-
3,4-Dichloranilid kyseliny cyklopropankarboxylove
n-(3,4-dichlorophenyl)cyclopropanecarboxamide[qr] | [Molecular Formula]
C10H9Cl2NO | [MDL Number]
MFCD00043471 | [MOL File]
2759-71-9.mol | [Molecular Weight]
230.09 |
| Chemical Properties | Back Directory | [Melting point ]
127-129 °C | [Boiling point ]
402.7±35.0 °C(Predicted) | [density ]
1.2791 (rough estimate) | [refractive index ]
1.5500 (estimate) | [pka]
13.33±0.70(Predicted) | [Henry's Law Constant]
3.8×103 mol/(m3Pa) at 25℃, HSDB (2015) | [EPA Substance Registry System]
Cypromid (2759-71-9) |
| Hazard Information | Back Directory | [Description]
Cypromid is an obsolete herbicide. It is moderately soluble in water but other data relevant to its environmental fate is unavailable. No data is available regarding its ecotoxicology. Cypromid has a low oral mammalian toxicity and is an irritant. | [Uses]
Cypromid is a herbicide. | [Definition]
ChEBI: Cypromid is an anilide. | [Production Methods]
Cypromid would have been manufactured using the same multipurpose plant processes applied to other acylanilide type herbicides of the 1960s–1980s. Industrial production began with preparation or procurement of the 3,4 dichloroaniline intermediate, which was then reacted with cyclopropanecarbonyl chloride (or an equivalent activated acid derivative) in a controlled acylation step to form the target cyclopropanecarboxanilide structure. This reaction required dry conditions, acid scavengers, and careful temperature control to manage hydrogen chloride evolution. The crude product was then subjected to neutralisation, solvent exchange, and crystallisation or vacuum drying to yield technical grade cypromid. | [Mechanism of action]
Contact; Selective, induces general necrosis and inhibits growth | [Pesticide Type]
Herbicide |
|
|