103361-09-7

Basic information

• Product Name: FLUMIOXAZIN
• Synonyms: N-(7-Fluoro-3,4-dihydro-3-oxo-(2-propynyl)-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboxamide;7-Fluoro-6-(3,4,5,6-tetrahydrophthalimido)-4-(2-propynyl)-1,4-benzoxazin-3(2H)-one;2-(7-Fluoro-3-oxo-4-prop-2-yn-1-yl-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione;Flumioxazin 100mg [103361-09-7];FluMinoxazin;2-[7-Fluoro-3,4-dihydro-3-oxo-4-(2-propyn-1-yl)-2H-1,4-benzoxazin-6-yl]-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione;FluMizin;Guillotine
• CAS NO: 103361-09-7
• Molecular Formula: C19H15FN2O4
• Molecular Weight: 354.33
• Product Categories: Agro-Products;Aromatics;Heterocycles
• Mol File: 103361-09-7.mol
• Article Data: 0

Chemical Properties

• Melting Point: 201.83-203.83°
• Boiling Point: 644.4 °C at 760 mmHg
• Flash Point: 343.5 °C
• Appearance: /
• Density: d20 1.5132 g/ml
• Vapor Pressure: 1.69E-16mmHg at 25°C
• Refractive Index: 1.661
• Storage Temp.: 0-6°C
• PKA: -0.01±0.20(Predicted)
• CAS DataBase Reference: FLUMIOXAZIN(CAS DataBase Reference)
• NIST Chemistry Reference: FLUMIOXAZIN(103361-09-7)
• EPA Substance Registry System: FLUMIOXAZIN(103361-09-7)

Safety Data

• Hazard Codes: T,N
• Statements: 61-50/53
• Safety Statements: 53-45-60-61
• RIDADR: UN 3077 9 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 103361-09-7(Hazardous Substances Data)

Usage

Description

FLUMIOXAZIN is a benzoxazinones-type herbicide used on soybeans, peanuts, orchard fruits and other crop. It is a diphenyl ether group G herbicide that functioning through inhibiting the protoorphyrinogen oxidase. As a light-dependent peroxidising herbicide (LDPH), it takes effect by blocking heme and chlorophyll biosynthesis resulting in the accumulation of phototoxic porphyrins, leading to the membrane damage and further killing the weeds.

Uses

Herbicide.

Metabolic pathway

When the rats are given a single oral dose of 14C-S- 53482, seven metabolites are identified in the urine and the feces. Alcohol derivatives and the acetoanilide derivative are isolated from the urine, and three sulfonic acid conjugates with a sulfonic acid group incorporated into the double bond of the 3,4,5,6- tetrahydrophthalimide moiety are isolated from the feces.

InChI:InChI=1/C19H15FN2O4/c1-2-7-21-15-9-14(13(20)8-16(15)26-10-17(21)23)22-18(24)11-5-3-4-6-12(11)19(22)25/h1,8-9H,3-7,10H2