To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

Triadimefon

From Wikipedia, the free encyclopedia

Triadimefon
Names
IUPAC name
1-(4-Chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)butan-2-one
Other names
Triadimeform
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.050.986 Edit this at Wikidata
UNII
  • InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3
    Key: WURBVZBTWMNKQT-UHFFFAOYSA-N
  • InChI=1/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3
    Key: WURBVZBTWMNKQT-UHFFFAOYAV
  • CC(C)(C)C(=O)C(N1C=NC=N1)OC2=CC=C(C=C2)Cl
Properties
C14H16ClN3O2
Molar mass 293.75 g·mol−1
Density 1.22 g/cm3[1]
Melting point 82 °C (180 °F; 355 K)[1]
Boiling point decomposes
64 mg/L (20 °C)[1]
Hazards
Lethal dose or concentration (LD, LC):
363 mg/kg (oral, rat)[1]
> 5000 mg/kg (dermal, rat)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Triadimefon is a fungicide used in agriculture to control various fungal diseases. As a seed treatment, it is used on barley, corn, cotton, oats, rye, sorghum, and wheat.[2] In fruit it is used on pineapple and banana.[2] Non-food uses include pine seedlings, Christmas trees, turf, ornamental plants, and landscaping.[2]

YouTube Encyclopedic

  • 1/3
    Views:
    1 204
    6 492
    611
  • Dwarfing effect on Adenium and overbearing effect on ficus attained by Gibberellin blocker
  • Control de Plagas y proceso de Fertilización en Cultivos de Café - TvAgro por Juan Gonzalo Angel
  • Malezas Mentales por Débora Chajet y Susana Chajet - Parte I

Transcription

References

  1. ^ a b c d e Record  in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  2. ^ a b c "Triadimefon Reregistration Eligibility Decision (RED) and Triadimenol Tolerance Reassessment and Risk Management Decision (TRED) Fact Sheet". Environmental Protection Agency.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 21 August 2023, at 18:22
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy