3-o-methylphenyl-2-oxo-1-oxaspiro[4,4]-n-3-ene-4-alcohol and derivatives thereof

A technology of o-methylphenyl and oxaspiro, which is applied in the directions of biocides, chemicals for biological control, biocides, etc., to achieve the effect of preventing damage

Active Publication Date: 2010-12-29
HUNAN CHEM RES INST
View PDF6 Cites 19 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although there are many pests, pest mites, and germ control agents on the market, due to the continuous expansion of the market, the resistance of pests, pest mites, and diseases, the service life of drugs, and the economics of drugs, and people's increasing emphasis on the environment , scientists need to continue to study, and then develop new efficient, safe, economical and different types of insecticides, miticides, and fungicides

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • 3-o-methylphenyl-2-oxo-1-oxaspiro[4,4]-n-3-ene-4-alcohol and derivatives thereof
  • 3-o-methylphenyl-2-oxo-1-oxaspiro[4,4]-n-3-ene-4-alcohol and derivatives thereof
  • 3-o-methylphenyl-2-oxo-1-oxaspiro[4,4]-n-3-ene-4-alcohol and derivatives thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

Embodiment 2

Embodiment 3

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
melting pointaaaaaaaaaa
melting pointaaaaaaaaaa
Login to view more

Abstract

The invention relates to 3-omethylphenyl-2-oxo-1-oxaspiro [4,4]-n-3-ene-4-alcohol which has a formula (I), derivatives and isomers thereof as well as preparation methods of the 3-omethylphenyl-2-oxo-1-oxaspiro [4,4]-n-3-ene-4-alcohol and the derivatives and the isomers thereof. The 3-omethylphenyl-2-oxo-1-oxaspiro [4,4]-n-3-ene-4-alcohol has the bioactivities of insect killing, mite killing and fungus killing.

Description

technical field The present invention relates to 3-o-methylphenyl-2-oxo-1-oxaspiro[4,4]-non-3-en-4-ol with insecticidal, acaricidal and fungicidal biological activities and its Derivatives and methods for their preparation. Background technique The control of pests, harmful mites and pathogens is very important in the process of realizing efficient agriculture. At the same time, the control of pests, harmful mites, and germs is also very important in forestry, animal husbandry, sideline, fishery, and public health. Although there are many pests, pest mites, and germ control agents on the market, due to the continuous expansion of the market and the problems of resistance to pests, pest mites, and diseases, the service life of drugs, and the economics of drugs and people's increasing emphasis on the environment , Scientists need to continue to study, and then develop new efficient, safe, economical and different types of insecticides, acaricides, and fungicides. Bayer com...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07D307/94A01N43/12A01P7/02A01P7/04A01P3/00
CPCA01N43/12A01N47/06C07D307/94A01N53/00
Inventor 柳爱平任叶果黄路裴晖胡志彬林雪梅成四喜黄明智祝小星韦天龙
Owner HUNAN CHEM RES INST
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products