60506-35-6

Basic information

• Product Name: 2-(2,4-DINITRO-PHENOXY)-ISOINDOLE-1,3-DIONE
• Synonyms: 2-(2,4-Dinitro-phenoxy)-isoindole-1,3-dione;2-(2,4-Dinitrophenoxy)isoindoline-1,3-dione;1H-Isoindole-1,3(2H)-dione, 2-(2,4-dinitrophenoxy)-;2-(2,4-dinitrophenoxy)-1H-isoindole-1,3(2H)-dione
• CAS NO: 60506-35-6
• Molecular Formula: C₁₄H₇N₃O₇
• Molecular Weight: 329
• Mol File: 60506-35-6.mol
• Article Data: 16

Chemical Properties

• Melting Point: 185-187 °C(Solv: acetone (67-64-1); methanol (67-56-1))
• Boiling Point: 531.8±60.0 °C(Predicted)
• Appearance: /
• Density: 1.681±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-(2,4-DINITRO-PHENOXY)-ISOINDOLE-1,3-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-DINITRO-PHENOXY)-ISOINDOLE-1,3-DIONE(60506-35-6)
• EPA Substance Registry System: 2-(2,4-DINITRO-PHENOXY)-ISOINDOLE-1,3-DIONE(60506-35-6)

Safety Data

• Hazardous Substances Data: 60506-35-6(Hazardous Substances Data)

Usage

General Description

2-(2,4-Dinitro-phenoxy)-isoindole-1,3-dione, also known as Isoxaben, is a synthetic chemical compound used as an herbicide to control the growth of unwanted plants. It works by inhibiting the growth of roots in germinating plants, preventing them from developing properly. Isoxaben is commonly used in agriculture and horticulture to control annual grasses and broadleaf weeds in various crops, including vegetables, fruits, ornamental plants, and turf. It is also used as a pre-emergence herbicide, meaning it is applied before the weeds germinate to prevent their growth. However, Isoxaben should be used with caution as it can be toxic to aquatic organisms and can pose risks to non-target plants.

InChI:InChI=1S/C14H7N3O7/c18-13-9-3-1-2-4-10(9)14(19)15(13)24-12-6-5-8(16(20)21)7-11(12)17(22)23/h1-7H

Upstream product

• 524-38-9 N-hydroxyphthalimide 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 584-48-5 2,4-dinitrobromobenzene 
• 97-00-7 1-chloro-2,4-dinitro-benzene 

Downstream Products

• 1313726-18-9 1-amino-4-((tert-butyldimethylsilyloxy)methyl)pyridinium 2,4-dinitrophenolate 
• 1198169-64-0 N-(4-(morpholinomethyl)thiazol-2-yl)-2-(3-(trifluoromethyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridine-8-carboxamide 
• 1198171-14-0 ethyl 2-(3-(trifluoromethyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridine-8-carboxylate 
• 1198171-16-2 2-(3-(trifluoromethyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridine-8-carboxylic acid 

Relevant articles and documents

SUBSTITUTED TETRAHYDROISOQUINOLINE ETHYLBENZAMIDE ANTI-CANCER AGENTS

The compounds herein disclosed are N-substituted tetrahydroisoquinoline ethylbenzamide compounds that have modifications on the phenyl rings by introducing groups with various electronic properties. These derivatives of N-substituted tetrahydroisoquinoline ethylbenzamide compounds have been shown to have anti-proliferative activity against cells. In particular, the compounds have been found to be effective in inhibiting the proliferation of cancer cells, such as cancer cells that originated in breast tissue. Additionally, it has been shown that the novel compounds have IC50 values against the breast cancer cells that are 6- to 10-fold less than the IC50 of Tamoxifen.

Enantioselective Synthesis of Chiral Oxime Ethers: Desymmetrization and Dynamic Kinetic Resolution of Substituted Cyclohexanones

Axially chiral cyclohexylidene oxime ethers exhibit unique chirality because of the restricted rotation of C=N. The first catalytic enantioselective synthesis of novel axially chiral cyclohexylidene oximes has been developed by catalytic desymmetrization of 4-substituted cyclohexanones with O-arylhydroxylamines and is catalyzed by a chiral BINOL-derived strontium phosphate with excellent yields and good enantioselectivities. In addition, chiral BINOL-derived phosphoric acid catalyzed dynamic kinetic resolution of α-substituted cyclohexanones has been performed and yields versatile intermediates in high yields and enantioselectivities.

PYRAZOLE-BASED COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME

The present invention relates to a pyrazole-based compound and an organic light emitting device comprising the same. The organic light emitting device comprises a positive electrode, a negative electrode, and one or more layers of organic layers formed between the positive electrode and the negative electrode, wherein one or more layers of organic layers comprise the pyrazole-based compound.COPYRIGHT KIPO 2015