152626-77-2

Usage

Uses

Used in Chemical Synthesis:
5-Amino-2-bromo-4-methylanisole is used as an intermediate compound for the synthesis of other chemicals. Its unique structure with a methoxy group and a bromine atom allows it to be a valuable building block in the production of various organic compounds.
Used in Laboratory Research:
5-Amino-2-bromo-4-methylanisole is used as a research compound in laboratories. Its properties and reactivity can be studied to understand its potential applications and to develop new methods for its synthesis or modification.
Note: Due to the limited information available about the specific uses of 5-Amino-2-bromo-4-methylanisole, the applications listed above are based on the general properties of anisoles and the potential uses of similar compounds. Further research and studies are needed to fully understand the applications and effects of this chemical compound.

Upstream product

• 871878-59-0 acetic acid-(4-bromo-5-methoxy-2-methyl-anilide) 
• 50868-75-2 5’-methoxy-2’-methylacetanilide 
• 134-19-0 2-methoxy-4-nitro-5-methyl aniline 
• 50868-72-9 5-methoxy-o-toluidine 

Downstream Products

• 1613504-91-8 C₂₀H₁₉F₃N₂O₂ 
• 152626-78-3 5-bromo-6-methoxy-1H-indazole 
• 1613505-31-9 6-cyclopropyl-5-(2-(trifluoromethyl)phenyl)-1H-indazole 
• 1613505-15-9 6-methoxy-5-(2-(trifluoromethyl)phenyl)-1H-indazole 
• 1613505-28-4 1-(tetrahydro-2H-pyran-2-yl)-5-(2-(trifluoromethyl)phenyl)-1H-indazol-6-ol 
• 1613505-29-5 1-(tetrahydro-2H-pyran-2-yl)-5-(2-(trifluoromethyl)phenyl)-1H-indazol-6-yl trifluoromethanesulfonate 
• 1613505-30-8 6-cyclopropyl-1-(tetrahydro-2H-pyran-2-yl)-5-(2-(trifluoromethyl)phenyl)-1H-indazole 
• 1613504-76-9 4-bromo-5-methoxy-2-methylbenzenediazonium tetrafluoroborate 

Relevant academic research and scientific papers

NEW COMPOUND AND USE THEREOF

PROBLEM TO BE SOLVED: To provide a compound for visualizing TRPA1 in an organism. SOLUTION: The invention provides a compound represented by the formula (1) or (2) in the figure or a salt thereof. (In the formulas, R1 and R2 are each a substituent having a radioisotope.) SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

MICROBIOCIDAL PHENYLAMIDINE DERIVATIVES

Compounds of the formula (I), wherein R1, R2, R3, R4 and R5 are as defined in claim 1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling infestation of plants, harvested food crops, seeds or non-living materials by phytopathogenic microorganisms, in particular fungi.

FUNGICIDAL COMPOSITIONS

A fungicidal composition comprising a mixture of a N-phenylamidine defined by formula (I) as component (A) and a further pesticide as component (B) as defined in claim 1, as well as the use of the composition in agriculture or horticulture for controlling or preventing infestation of plants by phytopathogenic microorganisms, preferably fungi.

MICROBIOCIDAL PHENYLAMIDINE DERIVATIVES

Compounds of the formula (I) wherein R1, R2, R3, R4, R5, R6, R7, R8 and X are as defined in claim 1. Furthermore, the present invention relates to agrochemical compositions which comprise compounds of formula (I), to preparation of these compositions, and to the use of the compounds or compositions in agriculture or horticulture for combating, preventing or controlling infestation of plants, harvested food crops, seeds or non-living materials by phytopathogenic microorganisms, in particular fungi.

Synthesis and reactivity of dimethoxy-functionalised Troeger's base analogues

Troeger's base analogues were prepared bearing methoxy groups in the 1,7-, 2,8-, 3,9- or 4,10-positions. These compounds were converted to their dihydroxy analogues in excellent yields upon treatment with boron tribromide and the 4,10-dihydroxy analogue could be prepared by directly from 4-hydroxyaniline. The synthetic utility of the dihydroxy-functionalised compounds as building blocks was demonstrated by the synthesis of a dialkoxy and a diester Troeger's base analogue.

Arylindazoles and their use as herbicides

This invention relates to substituted aryl indazoles, a process for producing them and their use as herbicides. In particular this invention relates to substituted aryl indazoles of the formula STR1 wherein all variables are as defined in the specification.