67747-01-7

Basic information

• Product Name: N-[2-(2,4,6-trichlorophenoxy)ethyl]propylamine
• Synonyms: N-[2-(2,4,6-trichlorophenoxy)ethyl]propylamine;N-(2,4,6-TRICHLORO PHENOXY)ETHYL N-PROPYL AMINE;2-(2,4,6-Trichlorophenoxy)ethylpropylamine;N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine;N-(2-(2,4,6-Trichlorophenoxy)ethyl)propan-1-aMine
• CAS NO: 67747-01-7
• Molecular Formula: C₁₁H₁₄Cl₃NO
• Molecular Weight: 282.59396
• EINECS: 266-992-4
• Mol File: 67747-01-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 361.1°C at 760 mmHg
• Flash Point: 172.2°C
• Appearance: /
• Density: 1.26g/cm³
• Vapor Pressure: 2.13E-05mmHg at 25°C
• Refractive Index: 1.534
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), DMSO (Slightlyu), Methanol (Slightly)
• PKA: 9.19±0.19(Predicted)
• CAS DataBase Reference: N-[2-(2,4,6-trichlorophenoxy)ethyl]propylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(2,4,6-trichlorophenoxy)ethyl]propylamine(67747-01-7)
• EPA Substance Registry System: N-[2-(2,4,6-trichlorophenoxy)ethyl]propylamine(67747-01-7)

Safety Data

• Hazardous Substances Data: 67747-01-7(Hazardous Substances Data)

Usage

Uses

N-(2-(2,4,6-Trichlorophenoxy)ethyl)propan-1-amine is a metabolite of Prochloraz which is a widely used imidazole fungicide.

InChI:InChI=1/C11H14Cl3NO/c1-2-3-15-4-5-16-11-9(13)6-8(12)7-10(11)14/h6-7,15H,2-5H2,1H3

Upstream product

• 107-10-8 propylamine 
• 13001-29-1 2-(2,4,6-trichlorophenoxy)-ethyl chloride 
• 106-94-5 propyl bromide 

Downstream Products

• 98156-27-5 Ethylchlor<<2-(2,4,6-trichlorphenoxy)-ethyl>-propylamido>phosphat 

Relevant articles and documents

Synthesis method of 2-(2,4,6-trichlorophenoxy)ethyl propylamine

The invention discloses a synthesis method of 2-(2,4,6-trichlorophenoxy)ethyl propylamine. The method comprises the following steps: reacting 2,4,6-trichlorophenol with cycloethylamine under the catalysis of boron trifluoride diethyl ether, and conducting salifying with hydrochloric acid to obtain a compound A; and under the catalysis of cesium hydroxide monohydrate, reacting the compound A with 1-bromopropane by taking sodium carbonate as an acid-binding agent to obtain 2-(2,4,6-trichlorophenoxy)ethyl propylamine. The method is simple in operation steps, the used reaction raw materials are cheap and easy to obtain, total molar yield is 94.18%, the purity of the produced 2-(2,4,6-trichlorophenoxy)ethyl propylamine is 98.0% or above, product quality is good, and the method is suitable for industrial production.

Substituted heteroaralkyl, heteroaralkenyl or halomethyl fungicides

Compounds of the formula: STR1 wherein R is phenyl or phenyl substituted with 1 to 4 of the same or different substituents selected from fluoro, chloro, bromo, iodo, lower alkyl and trihalomethyl; R1 is lower alkyl; Y is lower alkenyl substituted with a 5- or 6-member heterocyclic ring containing 1 to 3 nitrogen atoms and the remainder of the ring atoms carbon atoms, or --CH2 W wherein W is fluoro, chloro, bromo, iodo, or a 5- to 6-member heterocyclic ring containing 1 to 3 nitrogen atoms and the remainder of the ring atoms carbon atoms; and X and Z are independently sulfur or oxygen; are effective fungicides.

Certain N,N-di-substituted-pyridine carboxamides, fungicidal compositions and fungicidal method of use

The substituted heteroaryl compounds of this invention are good fungicides. In particular, they possess especially good activity against Bean Powdery Mildew.