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Quality Level
assay
≥99.0% (AT)
form
crystals
optical activity
[α]20/D −15.5±2°, c = 2% in H2O
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
SMILES string
Cl.COC(=O)[C@H](N)C(C)C
InChI
1S/C6H13NO2.ClH/c1-4(2)5(7)6(8)9-3;/h4-5H,7H2,1-3H3;1H/t5-;/m1./s1
InChI key
KUGLDBMQKZTXPW-NUBCRITNSA-N
Related Categories
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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Nature communications, 4, 2188-2188 (2013-07-19)
Enantiomeric excess of chiral compounds is a key parameter that determines their activity or therapeutic action. The current paradigm for rapid measurement of enantiomeric excess using NMR is based on the formation of diastereomeric complexes between the chiral analyte and
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