Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H23NO |
Molecular Weight | 197.3171 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCCCCCCCCCCN1
InChI
InChIKey=JHWNWJKBPDFINM-UHFFFAOYSA-N
InChI=1S/C12H23NO/c14-12-10-8-6-4-2-1-3-5-7-9-11-13-12/h1-11H2,(H,13,14)
Molecular Formula | C12H23NO |
Molecular Weight | 197.3171 |
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 |
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Development and validation of analytical methods for monomeric and oligomeric migrants from nylon 12 packaging materials. | 2003 Apr |
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Alternative fatty food simulants and diffusion kinetics of nylon 12 food packaging. | 2003 Oct |
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Vibrational and electronic couplings in ultraviolet resonance Raman spectra of cyclic peptides. | 2003 Sep |
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Cyanuric chloride as a mild and active Beckmann rearrangement catalyst. | 2005 Aug 17 |
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Reducing-difference infrared spectral analysis of cis- and trans-configurated lactams. | 2006 Feb |
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One-pot synthesis of lactams from cycloalkanes and tert-butyl nitrite by using N-hydroxyphthalimide as key catalyst. | 2006 Nov 20 |
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Beckmann rearrangement of ketoximes to lactams by triphosphazene catalyst. | 2008 Apr 4 |
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The screening, characterization, and use of omega-laurolactam hydrolase: a new enzymatic synthesis of 12-aminolauric acid. | 2008 Aug |
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High yield synthesis of 12-aminolauric acid by "enzymatic transcrystallization" of omega-laurolactam using omega-laurolactam hydrolase from Acidovorax sp. T31. | 2009 May |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:55:16 GMT 2023
by
admin
on
Fri Dec 15 17:55:16 GMT 2023
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Record UNII |
UB8VFC953G
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Record Status |
Validated (UNII)
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Record Version |
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C474694
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5774
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13690
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UB8VFC953G
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947-04-6
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77100
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213-424-8
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DTXSID1027344
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Laurolactam
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