60825-27-6

Basic information

• Product Name: Acetic acid, (3,5,6-trichloro-2-pyridinyl)oxy-, ethyl ester
• Synonyms: Acetic acid, (3,5,6-trichloro-2-pyridinyl)oxy-, ethyl ester;ethyl 2-(3,5,6-trichloropyridin-2-yl)oxyacetate
• CAS NO: 60825-27-6
• Molecular Formula: C9H8Cl3NO3
• Molecular Weight: 284.52
• Mol File: 60825-27-6.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 328.3°C at 760 mmHg
• Flash Point: 152.3°C
• Appearance: /
• Density: 1.455g/cm³
• Vapor Pressure: 0.000191mmHg at 25°C
• Refractive Index: 1.54
• PKA: -2.46±0.10(Predicted)
• CAS DataBase Reference: Acetic acid, (3,5,6-trichloro-2-pyridinyl)oxy-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, (3,5,6-trichloro-2-pyridinyl)oxy-, ethyl ester(60825-27-6)
• EPA Substance Registry System: Acetic acid, (3,5,6-trichloro-2-pyridinyl)oxy-, ethyl ester(60825-27-6)

Safety Data

• Hazardous Substances Data: 60825-27-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H8Cl3NO3/c1-2-15-7(14)4-16-9-6(11)3-5(10)8(12)13-9/h3H,2,4H2,1H3

Upstream product

• 105-39-5 chloroacetic acid ethyl ester 
• 6515-38-4 3,5,6-trichloropyridin-2 ol 
• 105-36-2 ethyl bromoacetate 
• 623-50-7 ethyl 2-hydroxyacetate 

Downstream Products

• 192445-28-6 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-phenyl-meth-(E)-ylidene]-hydrazide 
• 192445-60-6 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-o-tolyl-meth-(E)-ylidene]-hydrazide 
• 192445-66-2 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(3-chloro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-65-1 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(3-bromo-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-61-7 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-m-tolyl-meth-(E)-ylidene]-hydrazide 
• 192445-51-5 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-52-6 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(4-bromo-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-53-7 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-p-tolyl-meth-(E)-ylidene]-hydrazide 
• 192445-54-8 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-63-9 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(3-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-62-8 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(2-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-68-4 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(2-hydroxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-64-0 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(2-bromo-phenyl)-meth-(E)-ylidene]-hydrazide 
• 192445-57-1 (3,5,6-Trichloro-pyridin-2-yloxy)-acetic acid [1-(4-nitro-phenyl)-meth-(E)-ylidene]-hydrazide 

Relevant articles and documents

Novel 1,3,4-oxadiazole thioether derivatives containing flexible-chain moiety: Design, synthesis, nematocidal activities, and pesticide-likeness analysis

Seventy-two novel 1,3,4-oxadiazole thioether derivatives containing different flexible-chain moieties were designed and synthesized. The nematicidal activities of all the title compounds were evaluated, and some compounds showed excellent nematicidal acti

Method for preparing triclopyr 2-butoxyethyl ester

The invention discloses a method for preparing triclopyr 2-butoxyethyl ester. The method comprises the steps of dissolving sodium trichloro pyridinol by taking dimethyl formamide (DMF) as a solvent; dropwise adding ethyl chloroacetate and a catalyst and reacting to form an intermediate ethyl triclofenoxyacetate; carrying out filtering separation on the intermediate; and by taking methylbenzene asa solvent, adding butyl cellosolve and a catalyst to form the product triclopyr 2-butoxyethyl ester. The method has the advantages that the process flow is simple, the reaction time is short and the product can be obtained by only two-step reaction; in the reaction process, the amount of waste water is small and the process is highly environmentally friendly; a by-product produced by the reactionis ethanol which is safer and more environmentally friendly than methanol; and the total product yield is high and can be up to more than 88% and the product content can be up to more than 96%.

3, 5, 6-trichloro-2-pyridine phenoxyacetic acid derivatives preparation and applied research

The invention provides 3, 5, 6-trichlorine-2-pyridyloxyacetic acid derivatives which are soluble in both water and oil, have herbicidal activity and are shown as general formulas (I, II), wherein X refers to oxygen atoms, nitrogen atoms and sulfur atoms; n is 0, 1, 2, 3, 4, 5,..., or (CH2)n representing alkyl with a branched chain, wherein n refers to alkyl with a branched chain; Y refers to Cl-, Br-, F-, I-, AcO-, an acetylsalicylic acid radical, citric acid radical, salicylic acid radical, p-toluenesulfonic acid radical, hydrogen sulfate radical or other negative ions. R1 refers to alkyl with one to six carbon atoms, alkoxy with one to six carbon atoms, alkenyl with one to six carbon atoms, or aryl; R2 refers to alkyl with one to six carbon atoms, alkoxy with one to six carbon atoms, alkenyl with one to six carbon atoms or aryl groups; or R1 and R2 are selected from the structures shown in the specification.