5-ethyl-6-octyl-[1,2,3]triazolo[1,5-a]pyriMidin-7-aMine Chemical Properties

Melting point:

196 - 198°C

storage temp. 

-20°C Freezer, Under inert atmosphere

solubility 

Chloroform (Slightly, Sonicated), Dichloromethane (Slightly, Heated), DMSO (Slightly)

color 

White to Off-White

InChI

InChI=1S/C15H25N5/c1-3-5-6-7-8-9-10-12-13(4-2)19-15-17-11-18-20(15)14(12)16/h11H,3-10,16H2,1-2H3

InChIKey

GGKQIOFASHYUJZ-UHFFFAOYSA-N

SMILES

C12=NC=NN1C(N)=C(CCCCCCCC)C(CC)=N2

LogP

4.030 (est)

EPA Substance Registry System

[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine, 5-ethyl-6-octyl- (865318-97-4)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

WGK Germany 

3

Storage Class

11 - Combustible Solids

Hazard Classifications

Acute Tox. 4 Oral

5-ethyl-6-octyl-[1,2,3]triazolo[1,5-a]pyriMidin-7-aMine Usage And Synthesis

Uses

Ametoctradin acts as a pesticide, and is used in fomulations of insecticides and fungicides.

Definition

ChEBI: A member of the class of triazolopyrimidines that is [1,2,4]triazolo[1,5-a]pyrimidin-7-amine carrying additional ethyl and octyl substituents at positions 5 and 6 respectively. A fungicide for the control of late blight and downey mildew on po atoes and other crops including vines.

Synthesis

Ametoctradin (5-ethyl-6-octyl-[1,2,3]triazolo[1,5-a]pyriMidin-7-aMine) was synthesized through four steps from methyl 3-oxopentanoate and 1h-1,2,4-triazol-5-amine,and its structure was confirmed by 1h Nmr[1].

References

[1] Synthesis of Ametoctradin and Its Bioactivity. Proceedings of the 15th Annual Meeting of the Pesticide Professional Committee of the Chemical Industry and Engineering Society of China.

5-ethyl-6-octyl-[1,2,3]triazolo[1,5-a]pyriMidin-7-aMine(865318-97-4)Related Product Information

• TRIAZAMATE
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• Ametoctradin Metabolite 3
• Ametoctradin Metabolite 2
• Ametoctradin Metabolite 1
• Ametoctradin Metabolite 4