Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H6N4O |
| Molecular Weight | 102.0952 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=N)NC(N)=O
InChI
InChIKey=SQSPRWMERUQXNE-UHFFFAOYSA-N
InChI=1S/C2H6N4O/c3-1(4)6-2(5)7/h(H6,3,4,5,6,7)
| Molecular Formula | C2H6N4O |
| Molecular Weight | 102.0952 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Rapid liquid-phase combinatorial synthesis of heterocyclic libraries. | 2002 |
|
| Hydrogen bonding in 1-carbamoylguanidinium methylphosphonate monohydrate. | 2003 May |
|
| Preorganizing linear (self-complementary) quadruple hydrogen-bonding arrays using intramolecular hydrogen bonding as the sole force. | 2005 Nov 25 |
|
| Study of chemical stability of antivirally active 5-azacytosine acyclic nucleoside phosphonates using NMR spectroscopy. | 2008 Jul 15 |
|
| Products of the oxidation of 1-(diaminomethylene)thiourea with hydrogen peroxide. | 2008 Nov |
|
| Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp. | 2009 Dec 10 |
|
| Acyclic nucleoside phosphonates with 5-azacytosine base moiety substituted in C-6 position. | 2010 Jan 1 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:22:40 GMT 2023
by
admin
on
Sat Dec 16 08:22:40 GMT 2023
|
| Record UNII |
128C2R3P8G
|
| Record Status |
Validated (UNII)
|
| Record Version |
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128C2R3P8G
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141-83-3
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