Mefentrifluconazole Property

Boiling point:

518.7±60.0 °C(Predicted)

Density 

1.37±0.1 g/cm3(Predicted)

pka

12.68±0.29(Predicted)

form 

Solid

color 

Off-white to light yellow

EPA Substance Registry System

1H-1,2,4-Triazole-1-ethanol, .alpha.-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-.alpha.-methyl- (1417782-03-6)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Mefentrifluconazole Chemical Properties,Usage,Production

Description

Mefentrifluconazole is a C14-demethylation inhibitor in sterol biosynthesis，the first new isopropanol triazole fungicide developed and marketed by BASF. Mycloflunomide exhibits excellent biological properties, it is broad-spectrum, high-efficiency. Also It can prevent many fungal diseases such as rust and diseases caused by Ascidia.

Uses

Revysol is a useful research chemical compound used in the preparation of halogenalkylphenoxyphenyltriazolylethano??l derivatives for use as fungicides.

Definition

ChEBI: 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol is an aromatic ether that is diphenyl ether substituted by a 2-hydroxy-1-(1H-1,2,4-triazol-1-yl)propan-2-yl group at position 1, trifluoromethyl group at position 2 and a chloro group at position 4. It is a member of monochlorobenzenes, a member of triazoles, a tertiary alcohol, an aromatic ether and a member of (trifluoromethyl)benzenes.

Indications

Mefentrifluconazole is suitable for more than 60 kinds of crops, such as field crops, commercial crops and special crops. There are field crops such as corn, cereals, soybeans, rice, etc., as well as economic crops such as green peppers and grapes, and ornamental plants.

Synthesis

Mefentrifluconazole can be synthesized from 4-bromo-2-trifluoromethyl-1-iodobenzene via five steps of Grignard reaction, epoxidation, ring opening, boronation and deesterification.