| Identification | Back Directory | [Name]
CHLORANOCRYL | [CAS]
2164-09-2 | [Synonyms]
DCMA
Dicryl
licryl
n4,556
nia4556
fmc4556
N 4,556
DMCA(R)
FMC 4556
NIA 4556
DICRYL(R)
NIAGARA 4556
CHLORANOCRYL
Chloranocryl 0
dicryl (wssa, exansi)
chloranocryl (bsi,iso)
3',4'-Dichloromethacrylanilide
3',4'-Dichloro-2-methacrylanilide
3’,4’-dichloro-2-methacrylanilide
methacrylicacid3,4-dichloroanilide
3,4-dichloro-N-methacryloylaniline
3’,4’-dichloro-2-methyl-acrylanilid
3',4'-DICHLORO-2-METHYLACRYLANILIDE
Methacrylic Acid 3,4-dichloroanilide
N-(3,4-Dichlorophenyl)Methacrylamide
acrylanilide,3’,4’-dichloro-2-methyl-
3,4-dichloranilidkyselinymethakrylove
Acrylanilide, 3',4'-dichloro-2-methyl-
N-(3,4-DICHLOROPHENYL)METHYL-ACRYLAMIDE
3,4-Dichloranilid kyseliny methakrylove
CHLORANOCRYL PESTANAL (N-(3 4-DI-CHLORO&
2-Methyl-N-(3,4-dichlorophenyl)acrylamide
N-(3,4-Dichlorophenyl)-2-methylacrylamide
alpha-methylacrylicacid,3,4-dichloroanilide
n-(3,4-dichlorophenyl)-2-methyl-2-propenamid
n-(3,4-dichlorophenyl)-2-methyl-2-propenamide
alpha-Methylacrylic acid, 3,4-dichloroanilide
N-(3,4-dichlorophenyl)-2-methylprop-2-enamide
N-(3,4-dichlorophenyl)-2-methyl-prop-2-enamide
2-Propenamide, N-(3,4-dichlorophenyl)-2-methyl- | [Molecular Formula]
C10H9Cl2NO | [MDL Number]
MFCD00128007 | [MOL File]
2164-09-2.mol | [Molecular Weight]
230.09 |
| Hazard Information | Back Directory | [Description]
Chloranocryl is an obsolete contact herbicide. Little data is available regarding its environmenal fate, ecotoxicology or impact on human health. | [Chemical Properties]
White powder. Melting point 128°C. Insoluble in water, soluble in acetone (30%), pyridine (33%), dimethylformamide (51%), and xylene (25%). | [Uses]
Chloranocryl functions as a herbicide for agricultural purposes. | [Uses]
Herbicide. | [Definition]
ChEBI: Chloranocryl is an anilide. | [Production Methods]
Chloranocryl is produced through a multi step chemical synthesis typical of anilide herbicides. According to the synthesis data, the process begins with 3,4 dichloroaniline, which is reacted with methacryloyl chloride in a cooled polar solvent such as dimethylacetamide, with the temperature kept below 0 DegC to control reactivity. The mixture is then stirred at ambient temperature for an extended period to complete acylation, forming the key intermediate 3,4 dichloro N methacryloyl aniline. This intermediate is subsequently converted into the final herbicidal structure through additional steps involving epoxy acyl intermediates and solvent based purification. | [Mechanism of action]
Contact action. PSII inhibitor resulting in plant cell death and plant necrosis. | [Pesticide Type]
Herbicide |
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