Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H25NO |
| Molecular Weight | 199.333 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCC(N)=O
InChI
InChIKey=ILRSCQWREDREME-UHFFFAOYSA-N
InChI=1S/C12H25NO/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H2,13,14)
| Molecular Formula | C12H25NO |
| Molecular Weight | 199.333 |
| 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 |
|---|---|---|
| An investigation of dynamic surface tension, critical micelle concentration, and aggregation number of three nonionic surfactants using NMR, time-resolved fluorescence quenching, and maximum bubble pressure tensiometry. | 2003 Jun 15 |
|
| Fractionation, structural studies, and immunological characterization of the semi-synthetic Quillaja saponins derivative GPI-0100. | 2003 Sep 8 |
|
| Toxicological and metabolic investigations of the safety of N-alpha-lauroyl-L-arginine ethyl ester monohydrochloride (LAE). | 2004 Feb |
|
| A novel acylase from Streptomyces mobaraensis that efficiently catalyzes hydrolysis/synthesis of capsaicins as well as N-acyl-L-amino acids and N-acyl-peptides. | 2006 Jan 11 |
|
| Selective androgen receptor modulators in preclinical and clinical development. | 2008 |
|
| Lysosomes in iron metabolism, ageing and apoptosis. | 2008 Apr |
|
| Steady-state bioluminescence of bacterial luciferase using electrochemical regeneration of flavin substrate and its application to inhibitory analysis. | 2009 Apr |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:51:10 GMT 2023
by
admin
on
Fri Dec 15 15:51:10 GMT 2023
|
| Record UNII |
3BD22052MO
|
| Record Status |
Validated (UNII)
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| Record Version |
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214-298-7
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26630
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DTXSID5022146
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889
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14256
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3BD22052MO
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1120-16-7
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3BD22052MO
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34726
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