추천 제품
product name
N,N-Dimethyl-L-phenylalanine, 99%
Quality Level
분석
99%
형태
powder
광학 활성
[α]20/D +77°, c = 1.3 in H2O
반응 적합성
reaction type: solution phase peptide synthesis
mp
225-227 °C (lit.)
응용 분야
peptide synthesis
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
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애플리케이션
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
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.
Analytica Chimica Acta, 663(1), 109-116 (2010)
Total Synthesis of the Cyclopeptide Alkaloid Paliurine E. Insights into Macrocyclization by Ene? Enamide RCM.
The Journal of Organic Chemistry, 73(4), 1270-1281 (2008)
Synthesis of 5-(3-indolyl) oxazole natural products. Structure revision of Almazole D.
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.
Journal of Chromatography A, 1217(8), 1395-1398 (2010)
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