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.
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

Triazene

From Wikipedia, the free encyclopedia

Not to be confused with triazine or triazane.
Triazene
Structural formula of triazene
Space-filling model of the triazene molecule
Names
IUPAC name
Triazene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
49028
UNII
  • InChI=1S/H3N3/c1-3-2/h(H3,1,2) checkY
    Key: AYNNSCRYTDRFCP-UHFFFAOYSA-N checkY
  • NN=N
Properties
H3N3
Molar mass 45.045 g·mol−1
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability 4: Readily capable of detonation or explosive decomposition at normal temperatures and pressures. E.g. nitroglycerinSpecial hazards (white): no code
3
4
4
Related compounds
Other anions
 Triphosphane
Related Binary azanes
 ammonia
diazane
triazane
Related compounds
 Diazene
Tetrazene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
For organic derivatives, see triazenes.

Triazene is an unsaturated inorganic compound having the chemical formula N3H3. It has one double bond and is the second-simplest member of the azene class of hydronitrogen compounds, after diimide. Triazenes are a class of organic compounds containing the functional group -N(H)-N=N-. Triazene, possibly along with its isomer triimide (HNNHNH), has been synthesized in electron-irradiated ices of ammonia and ammonia/dinitrogen and detected in the gas phase after sublimation.[1]

YouTube Encyclopedic

  • 1/5
    Views:
    5 273
    3 669
    5 201
    66 930
    25 700
  • Triazines- Six membered heterocycle
  • Triazine
  • Triazine (6 Membered Heterocyclic compounds) SYNTHESIS & REACTION #heterocyclic #mscchemistrynotes
  • Which Chemical is the Most Uncanny?
  • Amine Regenerator

Transcription

References

  1. ^ Forstel, Tsegaw, Maksyutenko, Mebel, Sander, & Kaiser. "On the formation of N3H3 isomers in irradiated ammonia bearing ices: Triazene (H2NNNH) or Triimide (HNHNNH)", ChemPhysChem, 2016, 17, 2726.

External links

This page was last edited on 20 April 2024, at 16:24
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