Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C32H67N |
| Molecular Weight | 465.8811 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCC
InChI
InChIKey=NQYKSVOHDVVDOR-UHFFFAOYSA-N
InChI=1S/C32H67N/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h33H,3-32H2,1-2H3
| Molecular Formula | C32H67N |
| Molecular Weight | 465.8811 |
| 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 |
|---|---|---|
| Conductivity and viscosity behavior of asymmetric phosphonium iodides. | 2010-04-01 |
|
| Hydroacridines: part 29. 15N NMR chemical shifts of 9-substituted 1,2,3,4,5,6,7,8-octahydroacridines and their N-oxides-Taft, Swain-Lupton, and other types of linear correlations. | 2008-12 |
|
| Ab initio studies of solvent effect on molecular conformation and vibrational spectra of diacetamide. | 2004-04 |
|
| (1E)-2-(Diacetylamino)-1-methylprop-1-enyl acetate. | 2004-03 |
|
| Glycosylation of N-acetylglucosamine: imidate formation and unexpected conformation. | 2003-07-24 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:10:02 GMT 2025
by
admin
on
Mon Mar 31 21:10:02 GMT 2025
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| Record UNII |
05Y5G77L4R
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| Record Status |
Validated (UNII)
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| Record Version |
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