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About This Item
Empirical Formula (Hill Notation):
C11H14N2O
CAS Number:
Molecular Weight:
190.24
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
optical activity
[α]20/D −20.5°, c = 1 in methanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
73-77 °C (lit.)
application(s)
peptide synthesis
SMILES string
N[C@H](CO)Cc1c[nH]c2ccccc12
InChI
1S/C11H14N2O/c12-9(7-14)5-8-6-13-11-4-2-1-3-10(8)11/h1-4,6,9,13-14H,5,7,12H2/t9-/m0/s1
InChI key
UDQCRUSSQAXPJY-VIFPVBQESA-N
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E L Paley et al.
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The determination of enantiomeric excess (ee) in various groups of chiral compounds, namely amines, amino alcohols, diols, and hydroxy acids is performed using a dual chromophore FRET/PET based sensor ensemble. The sensing ensemble utilizes fluorescence changes from two chromophores (indicators)
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