Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C5H13NO |
Molecular Weight | 103.1628 |
Optical Activity | ( + ) |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)[C@H](N)CO
InChI
InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1
Molecular Formula | C5H13NO |
Molecular Weight | 103.1628 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The Bogorol family of antibiotics: template-based structure elucidation and a new approach to positioning enantiomeric pairs of amino acids. | 2006 Aug 4 |
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Invariom-model refinement of L-valinol. | 2006 Nov |
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Polymeric sulfated amino acid surfactants: a class of versatile chiral selectors for micellar electrokinetic chromatography (MEKC) and MEKC-MS. | 2007 Feb 1 |
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Amino acid derivatives from Lucilia sericata excretions/secretions may contribute to the beneficial effects of maggot therapy via increased angiogenesis. | 2010 Mar |
|
Synthesis of chiral β-aminoalcohol palladium complexes exhibiting cytotoxic properties. | 2010 Oct 14 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:46:36 GMT 2023
by
admin
on
Sat Dec 16 11:46:36 GMT 2023
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Record UNII |
R54N4NJ3ZZ
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Record Status |
Validated (UNII)
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Record Version |
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Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
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SALT/SOLVATE -> PARENT |
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