Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CN4 |
| Molecular Weight | 68.0375 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[N-]=[N+]=NC#N
InChI
InChIKey=KWEDUNSJJZVRKR-UHFFFAOYSA-N
InChI=1S/CN4/c2-1-4-5-3
| Molecular Formula | CN4 |
| Molecular Weight | 68.0375 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Thermal decomposition of NCN(3) as a high-temperature NCN radical source: singlet-triplet relaxation and absorption cross section of NCN((3)Σ). | 2010-12-23 |
|
| Carbonyl and oxalyl bridged bis(1,5-diaminotetrazole)-based energetic salts. | 2009-09-14 |
|
| 1-substituted 5-aminotetrazoles: syntheses from CNN3 with primary amines. | 2008-10-16 |
|
| Quantum chemical treatment of cyanogen azide and its univalent and divalent ionic forms. | 2008-05-30 |
|
| Synthesis of 1,2,3-triazole and 1,2,3,4-tetrazole-fused glycosides and nucleosides by an intramolecular 1,3-dipolar cycloaddition reaction. | 2008-02-21 |
|
| Linking cyano-bridged ladders by azide to form a layered metamagnet. | 2004-09-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:20:06 GMT 2025
by
admin
on
Mon Mar 31 21:20:06 GMT 2025
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| Record UNII |
159Y7EZP9V
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID30997772
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764-05-6
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159Y7EZP9V
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Cyanogen azide
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m3952
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admin on Mon Mar 31 21:20:06 GMT 2025 , Edited by admin on Mon Mar 31 21:20:06 GMT 2025
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PRIMARY | Merck Index |