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Mefentrifluconazole

Mefentrifluconazole Structure
CAS No.
1417782-03-6
Chemical Name:
Mefentrifluconazole
Synonyms
Mefentrifluconazole;2H3]-Mefentrifluconazole;Mefentrifluconazole (BAS-750F);2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol;2-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol;1H-1,2,4-Triazole-1-ethanol, α-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-α-methyl-;(2RS)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol: mefentrifluconazole;CYPs,aromatase,Inhibitor,antifungal,Fungal,Mefentrifluconazole,derivative,cell,azole,hypertrophy,liver,necrosis,Cytochrome P450,irritant,inhibit
CBNumber:
CB64745567
Molecular Formula:
C18H15ClF3N3O2
Molecular Weight:
397.78
MOL File:
1417782-03-6.mol
Modify Date:
2024/7/2 8:55:14

Mefentrifluconazole Properties

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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

Mefentrifluconazole Chemical Properties,Uses,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.

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.

Mefentrifluconazole Suppliers

Global( 33)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
Nextpeptide Inc +86-0571-81612335 +8613336028439 China 19915 58 Inquiry
InvivoChem +1-708-310-1919 +1-13798911105 United States 6393 58 Inquiry
Jilin Chinese Academy of Sciences-yanshen Technology +undefined18143011203 China 42057 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 52927 58 Inquiry
RD International Technology Co., Limited 18024082417 China 9268 58 Inquiry
Changzhou Chemscaler Pharmtech Co., Ltd. 0519-81096292 15312577869 China 305 60 Inquiry
InvivoChem 13549236410 China 6755 58 Inquiry
Wuhan TCASChem Technology Co., Ltd. 027-027-86697669 13986148687 China 3954 55 Inquiry
Shenzhen Regent Biochemical Technology Co., Ltd. 0755-0755-85201366 18938635012 China 9306 58 Inquiry

Related articles

Mefentrifluconazole 1H-1,2,4-Triazole-1-ethanol, α-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-α-methyl- Mefentrifluconazole (BAS-750F) (2RS)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol: mefentrifluconazole 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol 2-(4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol 2H3]-Mefentrifluconazole CYPs,aromatase,Inhibitor,antifungal,Fungal,Mefentrifluconazole,derivative,cell,azole,hypertrophy,liver,necrosis,Cytochrome P450,irritant,inhibit 1417782-03-6