Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H12N2O2 |
Molecular Weight | 144.1717 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)CCCCC(N)=O
InChI
InChIKey=GVNWZKBFMFUVNX-UHFFFAOYSA-N
InChI=1S/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10)
Molecular Formula | C6H12N2O2 |
Molecular Weight | 144.1717 |
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 |
---|---|---|
Mechanisms of suberoylanilide hydroxamic acid inhibition of mammary cell growth. | 2001 |
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Self-assembly and dynamics of [2]- and [3]rotaxanes with a dinuclear macrocycle containing reversible Os-N coordinate bonds. | 2001 Jun 18 |
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Differential evolution: crystal structure determination of a triclinic polymorph of adipamide from powder diffraction data. | 2002 Apr 21 |
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Development of biomimetic nano-hydroxyapatite/poly(hexamethylene adipamide) composites. | 2002 Dec |
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Efficient modulation of hydrogen-bonding interactions by remote substituents. | 2004 Jan 22 |
|
Water-in-oil gel emulsions from a cholesterol derivative: structure and unusual properties. | 2009 Aug 15 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:18:23 GMT 2023
by
admin
on
Fri Dec 15 17:18:23 GMT 2023
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Record UNII |
40DRU033OW
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Record Status |
Validated (UNII)
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Record Version |
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211-062-5
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628-94-4
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40DRU033OW
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7623
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5510
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12364
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C027486
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ADIPAMIDE
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DTXSID4020032
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