Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H20N2O |
| Molecular Weight | 172.2679 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCNC(=O)NCCCC
InChI
InChIKey=AQSQFWLMFCKKMG-UHFFFAOYSA-N
InChI=1S/C9H20N2O/c1-3-5-7-10-9(12)11-8-6-4-2/h3-8H2,1-2H3,(H2,10,11,12)
| Molecular Formula | C9H20N2O |
| Molecular Weight | 172.2679 |
| 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 |
|---|---|---|
| Intramolecular Michael addition reaction for the synthesis of benzylbutyrolactones. | 2010-07-21 |
|
| Synthesis of 5-vinylideneoxazolidin-2-ones by DBU-mediated CO2-fixation reaction of 4-(benzylamino)-2-butynyl carbonates and benzoates. | 2008-05-15 |
|
| Formulation factors that can reduce the formation of the phytotoxic impurity, N,N'-dibutylurea, from benomyl. | 2007-07 |
|
| DBU catalyzed cyanoacylation of ketones with acyl cyanides. | 2006-05-07 |
|
| Catalytic chemoselective addition of acetonitrile to enolizable aldehydes with cationic Ru complex/DBU combination. | 2005-07-28 |
|
| Accelerated degradation of N, N'-dibutylurea (DBU) upon repeated application. | 2005-06 |
|
| Functionalization of pyrimidine and purine nucleosides at C4 and C6: C-nucleophilic substitution of their C4- and C6-(1,2,4-triazol-1-yl) derivatives. | 2005 |
|
| Degradation of N,N'-dibutylurea (DBU) in soils treated with only DBU and DBU-fortified benlate fungicides. | 2004-09-10 |
|
| Assessing N,N'-Dibutylurea (DBU) formation in soils after application of n-butylisocyanate and benlate fungicides. | 2004-02-25 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:29:48 GMT 2025
by
admin
on
Mon Mar 31 19:29:48 GMT 2025
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| Record UNII |
J2HUG1I10W
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| Record Status |
Validated (UNII)
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| Record Version |
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