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PYROQUILON

PYROQUILON Structure
CAS No.
57369-32-1
Chemical Name:
PYROQUILON
Synonyms
CG 114;CORATOP;fongoren;cga49104;fongorene;Fungorene;FONGARENE;PYROQUILON;lilolidone;pyroquilone
CBNumber:
CB0470517
Molecular Formula:
C11H11NO
Molecular Weight:
173.21
MOL File:
57369-32-1.mol
Modify Date:
2023/8/17 13:38:56

PYROQUILON Properties

Melting point 112℃
Boiling point 355.2±42.0 °C(Predicted)
Density 1.25±0.1 g/cm3(Predicted)
vapor pressure 1.6 x 10-4 Pa (20 °C)
storage temp. 0-6°C
Water Solubility 4000 mg l-1 (20 °C)
pka 1.81±0.20(Predicted)
CAS DataBase Reference 57369-32-1

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H412
Precautionary statements  P273-P301+P312+P330
Hazard Codes  Xn
Risk Statements  22-52/53
Safety Statements  61
WGK Germany  2
RTECS  UY9480000
HS Code  29334900

PYROQUILON price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 45650 Pyroquilon PESTANAL?, analytical standard 57369-32-1 250MG ₹5098.58 2022-06-14 Buy
Product number Packaging Price Buy
45650 250MG ₹5098.58 Buy

PYROQUILON Chemical Properties,Uses,Production

Uses

Pyroquilon is used for the control of blast (Pyricularia oryzae) in rice.

Definition

ChEBI: A pyrroloquinoline that is 1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinoline in which the hydrogens at position 4 are replaced by an oxo group. A fungicide used to control rice blast, it is not approved wof use within the Eur pean Union.

Metabolic pathway

The fate of pyroquilon in rice and rats has been reported. Given the metabolic stability of cyclic amides, there are few options, other than hydroxylation, open for the metabolism of the compound. Its biotransformation involves initial hydroxylation at three sites in the molecule, followed by ring-opening, dehydration and further oxidation affording a somewhat complex picture. A study in rats revealed most of these metabolites but with some further metabolic degradation. The usual differences in conjugation were seen with mainly glucoside formation in plants and glucuronide and sulfate formation in animals.

Metabolism

Animals: Rapidly metabolized and eliminated via urine and feces. Residues in tissues were generally low, and there was no evidence for accumulation or retention of pyroquilon or its metabolites. Plants: Major metabolites in rice grain were 3,4-dihydro-4-hydroxy-2- oxoquinoline-8-acetic acid and two other acetic acid derivatives. Soil/Environment: DT50 (silty soil) 2, (sandy loam) 18 w. Kd 1.3–42 μg/g soil, little to moderately mobile. Photolysis in water, DT50 10 d.

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57369-32-1(PYROQUILON)Related Search:

PYROQUILON 2,1-ij)quinolin-4-one,1,2,5,6-tetrahydro-4h-pyrrolo( cga49104 fongoren fongorene lilolidone pyroquilone 1,2,5,6-TETRAHYDROPYRROL[3,2,1-IJ]QUINOLINE-4-ON PYROQUILON PESTANAL (1,2,5,6-TETRA- HYDR pyroquilon (bsi,draft-iso) pyroquilon (ISO) 1,2,5,6-tetrahydropyrrolo[3,2,1-ij]quinolin-4-one 1,2,5,6-Tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-4-one 4-Lilolidine Fungorene 1,2,5,6-TETRAHYDROPYRROLO(3,2,1-IJ)QUINOLIN-4-ONE Pyroquilon Standard 4,5-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-6(2H)-one CG 114 4-Oxo-1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinoline Pyroquilon 0.2 CORATOP FONGARENE 5,6-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-4(2H)-one Pyroquilon @100 μg/mL in Methanol Pyroquilon@1000 μg/mL in Acetonitrile 4H-Pyrrolo[3,2,1-ij]quinolin-4-one, 1,2,5,6-tetrahydro- 1-azatricyclo[6.3.1.0?12]dodeca-4(12),5,7-trien-11-one 57369-32-1 Alpha sort Fungicides N-PPesticides OthersAlphabetic P Pesticides&Metabolites PU - PZ