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ChemicalBook--->CAS DataBase List--->372137-35-4

372137-35-4

372137-35-4 Structure

372137-35-4 Structure
IdentificationBack Directory
[Name]

Saflufenacil
[CAS]

372137-35-4
[Synonyms]

Kixor
Saflufenacil
Kixor Herbicide
Saflufenacil@100 μg/mL in Methanol
Saflufenacil@1000 μg/mL in Acetonitrile
2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-...
Benzamide, 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]sulfonyl]-
[Molecular Formula]

C17H17ClF4N4O5S
[MDL Number]

MFCD16875523
[MOL File]

372137-35-4.mol
[Molecular Weight]

500.85
Chemical PropertiesBack Directory
[density ]

1.542±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO ()Slightly, Methanol (Slightly)
[form ]

neat
[pka]

4.24±0.40(Predicted)
[BRN ]

11326826
[InChI]

InChI=1S/C17H17ClF4N4O5S/c1-8(2)25(4)32(30,31)23-15(28)9-5-12(11(19)6-10(9)18)26-14(27)7-13(17(20,21)22)24(3)16(26)29/h5-8H,1-4H3,(H,23,28)
[InChIKey]

GNHDVXLWBQYPJE-UHFFFAOYSA-N
[SMILES]

C(NS(N(C)C(C)C)(=O)=O)(=O)C1=CC(N2C(=O)N(C)C(C(F)(F)F)=CC2=O)=C(F)C=C1Cl
[EPA Substance Registry System]

Benzamide, 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]sulfonyl]- (372137-35-4)
Safety DataBack Directory
[Symbol(GHS) ]


GHS09
[Signal word ]

Warning
[Hazard statements ]

H410
[Precautionary statements ]

P273-P391-P501
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

2
Hazard InformationBack Directory
[Uses]

Saflufenacil-d7 is the labeled version of Saflufenacil (S081800), which is a herbicide of the pyrimidinedione chemical class used for the preplant burndown and selective preemergence dicot weed control in different field crops. It was found to inhibit protoporphyrinogen IX oxidase (PPO) enzyme.
[Definition]

ChEBI: Saflufenacil is a member of the class of sulfamides that is sulfamide in which one of the amino groups has been substituted by a methyl group an an isopropyl group, while the other has been substituted by a 2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzoyl group. An important BASF herbicide, not registered in Europe but sold in USA, Canada and several other countries to control weeds in a wide range of food crops. Often mixed with other products such as glyphosate. It has a role as an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor, a herbicide and an agrochemical. It is a member of monochlorobenzenes, a member of monofluorobenzenes and a member of sulfamides. It is functionally related to a uracil.
[Mode of action]

Physiological and biochemical profiling confirmed that saflufenacil was a protoporphyrinogen-IX-oxidase (PPO) inhibitor. Saflufenacil elicits symptoms similar to other peroxidizing herbicides, including rapid, light-dependent necrosis of foliar tissue. Saflufenacil is readily absorbed by the root and shoot tissue of plants. Once absorbed, Saflufenacil is predominantly translocated via the xylem, with limited movement via the phloem. Saflufenacil is highly effective in controlling dicot weeds through contact and residual activity. In addition to non-crop and pre-plant burndown utility, saflufenacil demonstrates preemergence selectivity in a wide range of crops. Selectivity is conferred by physical placement and rapid metabolism of saflufenacil in tolerant crop species such as corn.
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