Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H10N2O |
| Molecular Weight | 102.135 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCNC(N)=O
InChI
InChIKey=ZQZJKHIIQFPZCS-UHFFFAOYSA-N
InChI=1S/C4H10N2O/c1-2-3-6-4(5)7/h2-3H2,1H3,(H3,5,6,7)
| Molecular Formula | C4H10N2O |
| Molecular Weight | 102.135 |
| 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 |
|---|---|---|
| Novel ureas and thioureas of 15-membered azalides with antibacterial activity against key respiratory pathogens. | 2009-09 |
|
| Palladium nanoclusters supported on propylurea-modified siliceous mesocellular foam for coupling and hydrogenation reactions. | 2008 |
|
| Synthesis and biological evaluation of new symmetrical derivatives as cytotoxic agents and apoptosis inducers. | 2005-03-15 |
|
| Discovery of N-propylurea 3-benzylpiperidines as selective CC chemokine receptor-3 (CCR3) antagonists. | 2004-04-05 |
|
| Controlling the selectivity of competitive nitroaldol condensation by using a bifunctionalized mesoporous silica nanosphere-based catalytic system. | 2004-02-04 |
|
| Inhibition of HIV-1 infection by alkylureas. | 1991-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:18:09 GMT 2025
by
admin
on
Mon Mar 31 19:18:09 GMT 2025
|
| Record UNII |
0PK51J4AV7
|
| Record Status |
Validated (UNII)
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| Record Version |
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627-06-5
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C017680
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73471
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DTXSID2060830
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210-981-9
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0PK51J4AV7
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