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ChemicalBook--->CAS DataBase List--->13360-45-7

13360-45-7

13360-45-7 Structure

13360-45-7 Structure
IdentificationBack Directory
[Name]

CHLORBROMURON
[CAS]

13360-45-7
[Synonyms]

C 6313
MALORAN
ciba6313
CIBA 6313
MALORAN(R)
'LGC' (1401)
CHLORBROMURON
CHLOROBROMURON
CHLOROBROMOURON
Chlorobromourone
Bromex(herbicide)
CHLORBROMURON STANDARD
CHLORBROMURON, 1GM, NEAT
CHLORBROMURON PESTANAL, 250 MG
Chlorbromuron 1g [13360-45-7]
3-Bromo-4-chlorofuran-2(5H)-one
Chlorbromuron 100 μg/mL in MeOH
chlorbromuron (bsi,iso,wssa,ansi)
3-(4-BROMO-3-CHLORPHENYL)-1-METHOXY-1-METHYLUREA
3-[4-BROMO-3-CHLOROPHENYL]-1-METHOXY-1-METHYLUREA
1-(3-Chloro-4-bromophenyl)-3-methyl-3-methoxyurea
3-(4-bromo-3-chlorophenyl)-1-methoxy-1-methyl-ure
1-(4-Bromo-3-chlorophenyl)-3-methoxy-3-methylurea
3-(3-Chloro-4-bromophenyl)-1-methoxy-1-methylurea
3-(3-Chloro-4-bromophenyl)-1-methyl-1-methoxyurea
N'-(4-Bromo-3-chlorophenyl)-N-methoxy-N-methylurea
n’-(4-bromo-3-chlorophenyl)-n-methoxy-n-methyl-ure
N-(4-Bromo-3-chlorophenyl)-N'-methoxy-N'-methylurea
n-(4-bromo-3-chlorophenyl)-n’-methoxy-n’-methylurea
Urea, 3-(4-bromo-3-chlorophenyl)-1-methoxy-1-methyl-
Urea, N'-(4-bromo-3-chlorophenyl)-N-methoxy-N-methyl-
[EINECS(EC#)]

236-411-9
[Molecular Formula]

C9H10BrClN2O2
[MDL Number]

MFCD00055474
[MOL File]

13360-45-7.mol
[Molecular Weight]

293.54
Chemical PropertiesBack Directory
[Melting point ]

95-97℃
[density ]

1.623
[refractive index ]

1.6160 (estimate)
[form ]

neat
[pka]

12.13±0.70(Predicted)
[Water Solubility ]

35.29mg/L(20 ºC)
[BRN ]

2128736
[EPA Substance Registry System]

Chlorbromuron (13360-45-7)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/38-36
[Safety Statements ]

26
[WGK Germany ]

2
[RTECS ]

YS2800000
[HS Code ]

29280000
[Hazardous Substances Data]

13360-45-7(Hazardous Substances Data)
[Toxicity]

rabbit,LD50,skin,> 10gm/kg (10000mg/kg),Ciba-Geigy Toxicology Data/Indexes. Vol. -, Pg. -, 1977.
Hazard InformationBack Directory
[Definition]

ChEBI: Chlorbromuron is a member of ureas.
[Metabolic pathway]

The main photoproducts initially formed in the phototransformation of linuron and chlorbromuron in aqueous solution result from photolysis, i.e. hydroxylation with release of the halide ion, and from elimination of a methoxy group. The orientation of the reaction depends on the wavelength: short wavelengths (254 nm) favor demethoxylation and photolysis in the meta position,whereas, with black light longer than 330 nm, photolysis in the para position is the main reaction observed. In soils, 4-bromo-3-chloroaniline is identified as a soil degradation product of chlorbromuron.
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