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 Structure
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)
pka1.20±0.40(Predicted)
form neat
color Pale Brown to Light Brown
Water Solubility 38mg/L at 25℃
BRN 4190275
LogP2.6 at 25℃
CAS DataBase Reference98730-04-2(CAS DataBase Reference)
NIST Chemistry ReferenceBenoxacor(98730-04-2)
EPA Substance Registry SystemBenoxacor (98730-04-2)
Safety Information
WGK Germany 2
RTECS DM3029000
HS Code 29349990
ToxicityLD50 (mg/kg): >5000 orally in rats; >2010 dermally in rabbits; LC50 in rats (mg/l): >2000 by inhalation (Fed. Regist.)
MSDS Information
Benoxacor Usage And Synthesis
UsesHerbicide safener.
UsesBenoxacor is a herbicide used as a part of pesticidal compositions.
DefinitionChEBI: Benoxacor is a benzoxazine.
Flammability and ExplosibilityNonflammable
Metabolic pathwayIn 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
2-CHLORO-N-(2-ETHOXYPHENYL)ACETAMIDE Methyl 2H-1,4-Benzoxazine, 4-(chloroacetyl)-3,4-dihydro- (8CI,9CI) Cloquintocet-mexyl FENCHLORAZOLE 2-(2-CHLOROETHYL)METHYLAMINOETHANOLHYDROCHLORIDE Dichloromethylvinylsilane Basic Violet 1 Dichloromethylphenylsilane Kresoxim-methyl Mefenpyr-diethyl alpha,alpha'-Dichloro-p-xylene 3-METHYL-3,4-DIHYDRO-2H-1,4-BENZOXAZINE Methyl acrylate Dihydromyrcenol Methyl acetate Benoxacor Propachlor

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