25141-25-7

Usage

Uses

Used in Agricultural and Gardening Applications:
2-(2,4-dinitrophenoxy)acetic acid is used as a herbicide for its effectiveness in controlling a wide variety of broadleaf weeds, which is crucial for maintaining the health and productivity of crops and gardens. Its application helps in reducing the competition for nutrients and space, thereby promoting the growth of desired plant species.
However, due to its highly toxic nature, the use of 2-(2,4-dinitrophenoxy)acetic acid has been significantly restricted in many countries to mitigate potential health hazards. Exposure to 2-(2,4-dinitrophenoxy)acetic acid can lead to skin irritation, respiratory issues, and central nervous system effects if not properly controlled. As a result, it is essential to follow safety guidelines and regulations when using dinoseb in agricultural and gardening practices.

InChI:InChI=1/C8H6N2O7/c11-8(12)4-17-7-2-1-5(9(13)14)3-6(7)10(15)16/h1-3H,4H2,(H,11,12)

Upstream product

• 19360-67-9 4-carboxymethoxy-benzoic acid 
• 51-28-5 2,4-Dinitrophenol 
• 79-11-8 chloroacetic acid 
• 7697-37-2 nitric acid 
• 122-59-8 2-phenoxyacetic acid 
• 7664-93-9 sulfuric acid 
• 99-96-7 4-hydroxy-benzoic acid 
• 584-48-5 2,4-dinitrobromobenzene 
• 25253-99-0 4-carboxymethoxy-3-nitro-benzoic acid 
• 3926-62-3 sodium monochloroacetic acid 

Downstream Products

• 55796-11-7 (2,4-dinitro-phenoxy)-acetic acid methyl ester 
• 85196-33-4 ethyl 2,4-dinitrophenoxyacetate 
• 89976-75-0 6-amino-2H-1,4-benzoxazin-3(4H)-one 
• 64490-03-5 2,4-dinitrophenoxyacetyl chloride 
• 139004-62-9 2-(2,4-Dinitro-phenoxy)-1-pyrazol-1-yl-ethanone 
• 139024-33-2 2-(2,4-Dinitro-phenoxy)-1-imidazol-1-yl-ethanone 
• 139004-67-4 2-(2,4-Dinitro-phenoxy)-1-morpholin-4-yl-ethanone 
• 72757-46-1 (2,4-dinitro-phenoxy)-acetic acid amide 
• 90814-94-1 N-(3-oxo-3,4-dihydro-2H-benz[1,4]oxazin-6-yl)-benzamide 

Relevant academic research and scientific papers

EGFR-targeting fluorescence quenching probe and preparation method and application thereof

The invention relates to the technical field of molecular probes, and discloses an EGFR-targeting fluorescence quenching probe and a preparation method and application thereof. The fluorescence quenching probe structurally comprises a pharmacodynamic skeleton structure, a fluorescence quenching group and a fluorescence labeling group, wherein the fluorescence labeling group is selected from BODIPYFL dye; and the fluorescence quenching group is selected from 2, 4-dinitrophenol. The pharmacodynamic skeleton structure can be combined with EGFR protein in a targeting mode, and when the quenchinggroup in the molecular probe leaves, the fluorescence labeling group can conduct specific tracing and imaging; and by means of molecular imaging, the expression process of specific cells and moleculescan be observed in real time, a target spot is traced, and therefore disease development status evaluation and accurate detection of EGFR mutation typing of lung cancer patients are achieved at the molecular pathological level.

A general approach for the development of fluorogenic probes suitable for no-wash imaging of kinases in live cells

A general approach is presented for developing small molecule-based fluorogenic probes suitable for no-wash imaging of endogenous kinases in live cells. Probe 1, including a fluorophore-quencher system, was only turned on upon reacting with its target kinase Btk, and disclosed Btk's cellular location in live cells without any washing.