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Diazynium

Base Information
  • Chemical Name:Diazynium
  • CAS No.:28647-38-3
  • Molecular Formula:H2N2
  • Molecular Weight:30.0293
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90951315
  • Nikkaji Number:J1.864.993D
  • Wikipedia:Isodiazene
  • Wikidata:Q3026454
Diazynium

Synonyms:diazynium;azanylidyneazanium;Isodiazene;Diazonium;28647-38-3;Nitrogen, ion;H2N.equiv.N;dinitrogen (1+)ion;HN2+;CHEBI:30102;DTXSID90951315;N#NH(+);N2+;Q3026454

Suppliers and Price of Diazynium
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Diazynium
Chemical Property:
  • Vapor Pressure:431000mmHg at 25°C 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:g/cm3 
  • XLogP3:1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:29.013973040
  • Heavy Atom Count:2
  • Complexity:8
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:[NH+]#N
Technology Process of Diazynium

There total 2 articles about Diazynium which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In further solvent(s); byproducts: N2, CO; Irradiation (UV/VIS); irradn. with a 1000-W Xenon lamp (Corning filters SC-7-54) in 2-methyltetrahydrofuran at 80 K; not isolated, detected by UV, IR;
DOI:10.1021/ja00328a076
Guidance literature:
In solid matrix; Irradiation (UV/VIS); photolysis of aminoisocyanate at 313 or 254 nm; isolated in Ar matrix at 12 K;
upstream raw materials:

carbamoyl azide

aminoisocyanate

Refernces

Facile synthesis of electrophilic vinyl boranes: Reactions of alkynyl-borates and diazonium salts

10.1039/c2cc35553a

The research focuses on the facile synthesis of electrophilic vinyl boranes. The purpose of this study is to develop an efficient and rapid method for producing substituted electrophilic vinyl boranes, which are significant molecules used as alkyl-abstraction reagents and Lewis acid catalysts in various applications, including olefin polymerization and hydrosilylation reactions. The researchers aimed to overcome the limitations of existing synthetic pathways, which are often plagued by challenging syntheses and low yields. The key chemicals used in this process include alkynylborate salts, which are derived from the reaction of frustrated Lewis pairs with terminal alkynes, and diazonium salts.

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