- Benoxacor
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- $11.00 / 1KG
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2019-07-06
- CAS: 98730-04-2
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 1000KG
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| | 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) | | Fp | >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) |
| WGK Germany | 2 | | RTECS | DM3029000 | | HS Code | 29349990 | | Toxicity | LD50 (mg/kg): >5000 orally in rats; >2010 dermally in rabbits; LC50 in rats (mg/l): >2000 by inhalation (Fed. Regist.) |
| | 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. |
| | Benoxacor Preparation Products And Raw materials |
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