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About This Item
Linear Formula:
C6H5CH2CH[N(CH3)2]CO2H
CAS Number:
Molecular Weight:
193.24
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
Beilstein/REAXYS Number:
2966581
MDL number:
Product Name
N,N-Dimethyl-L-phenylalanine, 99%
form
powder
SMILES string
CN(C)[C@@H](Cc1ccccc1)C(O)=O
InChI
1S/C11H15NO2/c1-12(2)10(11(13)14)8-9-6-4-3-5-7-9/h3-7,10H,8H2,1-2H3,(H,13,14)/t10-/m0/s1
InChI key
HOGIQTACRLIOHC-JTQLQIEISA-N
assay
99%
optical activity
[α]20/D +77°, c = 1.3 in H2O
reaction suitability
reaction type: solution phase peptide synthesis
mp
225-227 °C (lit.)
application(s)
peptide synthesis
Quality Level
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Application
N,N-Dimethyl-L-phenylalanine is commonly used to prepare Cu(II)-L-amino acid complex, which is a chiral mobile phase additive for the resolution of enantiomers. It can also be used in the total synthesis of (−)-paliurine E and almazole D.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis of 5-(3-indolyl) oxazole natural products. Structure revision of Almazole D.
Miyake F, et al.
Tetrahedron, 66(26), 4888-4893 (2010)
Different approaches of impregnation for resolution of enantiomers of atenolol, propranolol and salbutamol using Cu (II)-l-amino acid complexes for ligand exchange on commercial thin layer chromatographic plates.
Bhushan R and Tanwar S
Journal of Chromatography A, 1217(8), 1395-1398 (2010)
Non-ionic surfactant modified ligand exchange chromatography using copper (II) complex of N, N-dimethyl-l-phenylalanine as the chiral additive for enantioselective amino acids separation.
Dimitrova P and Bart H J
Analytica Chimica Acta, 663(1), 109-116 (2010)
Total Synthesis of the Cyclopeptide Alkaloid Paliurine E. Insights into Macrocyclization by Ene? Enamide RCM.
Toumi M, et al.
The Journal of Organic Chemistry, 73(4), 1270-1281 (2008)
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