72619-32-0

Basic information

• Product Name: 2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester
• Synonyms: (R)-Methyl 2-(4-((3-chloro-5-(trifluoroMethyl)pyridin-2-yl)oxy)phenoxy)propanoate;Haloxyfop P-Meth;Haloxyfop-R-me;(R)-Haloxyfop-p-methyl este;HALOXYFOP-P-METHYL;HALOXYFOP-R-METHYL;Methyl (R)-2-(4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propionate;2-(4-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester
• CAS NO: 72619-32-0
• Molecular Formula: C₁₆H₁₃ClF₃NO₄
• Molecular Weight: 375.73
• EINECS: 406-250-0
• Mol File: 72619-32-0.mol

Chemical Properties

• Boiling Point: 390.818 °C at 760 mmHg
• Flash Point: 2 °C
• Appearance: light brown to red brown sticky liquid
• Density: 0.968
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.513
• Storage Temp.: 2-8°C
• PKA: -1.52±0.32(Predicted)
• Water Solubility: 8.74 mg/L at 20 ºC
• CAS DataBase Reference: 2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester(72619-32-0)
• EPA Substance Registry System: 2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester(72619-32-0)

Safety Data

• Hazard Codes: Xn;N,N,Xn,F
• Statements: 22-50/53-36-20/21/22-11
• Safety Statements: 2-60-61-36/37-26-16
• RIDADR: UN1648 3/PG 2
• WGK Germany: 3
• Hazardous Substances Data: 72619-32-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester is used as a research compound for exploring its potential therapeutic uses in the pharmaceutical industry. Its unique structure and properties make it a candidate for the development of new drugs targeting various diseases and conditions.
Used in Chemical Synthesis:
In the chemical industry, 2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester serves as an intermediate in the synthesis of other complex organic molecules. Its reactivity and functional groups make it a valuable building block for creating a wide range of chemical products.
Used in Material Science:
2-(4-((3-Chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoic acid methyl ester may also find applications in material science, where its specific properties can be utilized to develop new materials with unique characteristics. Its potential use in this field is currently under investigation by researchers.

InChI:InChI=1/C16H13ClF3NO4/c1-9(15(22)23-2)24-11-3-5-12(6-4-11)25-14-13(17)7-10(8-21-14)16(18,19)20/h3-9H,1-2H3/t9-/m1/s1

Upstream product

• 67-56-1 methanol 
• 72537-17-8 2-fluoro-3-chloro-5-(trifluoromethyl)pyridine 
• 94050-90-5 (R)-2-(4-hydroxyphenoxy)propionic acid 

Downstream Products

• 95977-29-0 (R)-2-[4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenoxy]propanoic acid 

Relevant articles and documents

A new method for one-pot synthesis of aryloxyphenoxypropionate herbicides using 2,4,6-trichloro-1,3,5-triazine and (n-BU)4NI as a homogeneous catalyst

The one-pot reaction of halo-heterocycle, (R)-4-hydroxyphenoxy propionic acid and an alcohol, amine or sulfonamide is described as an efficient method for the synthesis of aryloxyphenoxy propionate hrerbicides by using 2,4,6-trichloro-1,3,5-triazine in the presence of (n-BU) 4NI, as a homogeneous catalyst under mild conditions. The present procedure offers several advantages, such as good yields, short reaction times and easy workup.

Herbicidal mixtures having a synergistic effect

PCT No. PCT/EP96/03996 Sec. 371 Date Feb. 17, 1998 Sec. 102(e) Date Feb. 17, 1998 PCT Filed Sep. 12, 1996 PCT Pub. No. WO97/10714 PCT Pub. Date Mar. 27, 1997A composition comprising at least one sulfonylurea of the formula I wherein R1 is substituted alkyl; halogen; a group ER6 (E=O, S or NR7); COOR8; NO2; S(O)oR9; SO2NR10R11; or CONR10R11; R2 is hydrogen, alkyl, alkenyl, alkynyl, halogen, alkoxy, haloalkoxy, haloalkyl, alkylsulfonyl, nitro, cyano or alkylthio; R3 is F, CF3, CF2Cl, CF2H, OCF3, OCF2Cl, or, if R1 is CO2CH3 and R2 is simultaneously fluorine, R3 is Cl, or, if R1 is CH2CF3 or CF2CF3, R3 is methyl, or, if R4 is OCF3 or OCF2Cl, R3 is OCF2H or OCF2Br; R4 is alkoxy, alkyl, alkylthio, alkylamino, dialkylamino, halogen, haloalkyl or haloalkoxy; and R5 is hydrogen, alkoxy or alkyl; or an enviromentally compatible salt of I, and an aryloxyalkanoic acid selected from the group consisting of 2,4-D, 2,4-DB, clomeprop, dichlorprop, dichlorprop-P, dichlorprop-P (2,4-DP-P), fenoprop (2,4,5-TP), fluoroxypyr, MCPA, MCPB, mecoprop, mecoprop-P, napropamide, napropanilide, triclopyr, and an enviromentally compatible salt thereof exhibits a synergistic herbicidal effect.