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About This Item
Linear Formula:
(CH3)2CHCH(NH2)COOCH3 · HCl
CAS Number:
Molecular Weight:
167.63
Beilstein:
3912091
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
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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
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Jan Labuta et al.
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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