1314008-27-9
Chemical Structure
Ipflufenoquin
- CAS No.: 1314008-27-9
- Formula:C19H16F3NO2
- Molecular Weight:347.33
IUPAC Name: 2-(2-((7,8-difluoro-2-methylquinolin-3-yl)oxy)-6-fluorophenyl)propan-2-ol
InChIKey: DSXOWZNZGWXWMX-UHFFFAOYSA-N
SMILES: OC(C)(C)C1=C(F)C=CC=C1OC2=CC3=CC=C(F)C(F)=C3N=C2C
Biological Activity: Ipflufenoquin is an insecticide with the potential to control primary infection with apple scab. Ipflufenoquin should be applied between half an inch of green and fruit set[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Ipflufenoquin | 99.78% | Ipflufenoquin is an insecticide with the potential to control primary infection with apple scab. Ipflufenoquin should be applied between half an inch of green and fruit set. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Ipflufenoquin (Standard) | ≥98% | (R)-Omeprazole (sodium) (Standard) is the analytical standard of (R)-Omeprazole (sodium). This product is intended for research and analytical applications. (R)-Omeprazole sodium is a gastric acid resistant compound with activity to inhibit gastric acid secretion. (R)-Omeprazole sodium is metabolized in vivo, and its metabolism is primarily affected by cytochrome P450 enzymes. The interaction between (R)-Omeprazole sodium and mannitol may affect its bioavailability in formulations. (R)-Omeprazole sodium exhibits reversible direct and metabolism-dependent inhibition of CYP2C19. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||