Benoxacor
Benoxacor Basic information
- Product Name:
- Benoxacor
- Synonyms:
-
- 2-PHENYL-4,6-DICHLORO PYRIMIDINE
- BENOXACOR
- SOFIT
- (+-)-2,2-dichloro-1-(3,4-dihydro-3-methyl-2h-1,4-benzoxazin-4-yl)ethanone
- (+-)-4-(dichloroacetyl)-3,4-dihydro-3-methyl-2h-1,4-benzoxazine
- 4-dihydro-3-methyl-4-benzoxazin(+-)-2h-4-(dichloroacetyl)-3
- (±)2,2-dichloro-1-(3,4-dichloro-3-methyl-2H-1，4-bensoxazin-4-yl)ethanone
- primextras
- CAS:
- 98730-04-2
- MF:
- C11H11Cl2NO2
- MW:
- 260.12
- EINECS:
- 619-372-6
- Product Categories:
-
- A-BAlphabetic
- Alpha sort
- B
- BA - BH
- Pesticides&Metabolites
- Mol File:
- 98730-04-2.mol
Benoxacor Chemical Properties
- Melting point:
- 105-107°
- Boiling point:
- 240°C (rough estimate)
- Density
- 1.3416 (rough estimate)
- vapor pressure
- 0.002Pa at 25℃
- refractive index
- 1.6070 (estimate)
- Flash point:
- >107 °C
- storage temp.
- 0-6°C
- solubility
- Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
- pka
- 1.20±0.40(Predicted)
- color
- Pale Brown to Light Brown
- Water Solubility
- 38mg/L at 25℃
- BRN
- 4190275
- LogP
- 2.6 at 25℃
- CAS DataBase Reference
- 98730-04-2(CAS DataBase Reference)
- NIST Chemistry Reference
- Benoxacor(98730-04-2)
- EPA Substance Registry System
- Benoxacor (98730-04-2)
Benoxacor Usage And Synthesis
Uses
Benoxacor is a herbicide used as a part of pesticidal compositions.
Uses
Herbicide safener.
Definition
ChEBI: Benoxacor is a benzoxazine.
Flammability and Explosibility
Non flammable
Metabolic pathway
In cell suspension cultures of corn (Zea mays) with 14C-benoxacor, benoxacor is rapidly metabolized to six detectable metabolites within 0.5 h. Twelve metabolites are detected in extracts from the treated cells for 24 h. Of the three predominant metabolites present, two metabolites are the catabolic formylcarboxamide and carboxycarboxamide derivatives of benoxacor. The third one is the mono glutathione conjugate of benoxacor. This metabolite consists of a single glutathione molecule linked via the cysteinyl sulfhydryl group to the N-dichloroacetyl a- carbon of benoxacor. A catabolic a-hydroxyacetamide derivative is detected as well as its amino acid conjugates either containing glutathione residue or presumably derived from the glutathione residue. A disaccharide conjugate is identified as S-(O-diglycoside)glutathione conjugate.
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