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N-Boc-L-phenylalanine, 99%, Thermo Scientific Chemicals
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Catalog number A16017.14
also known as A16017-14
Price (USD)/ Each
146.00
-
Quantity:
25 g
Price (USD)/ Each
146.00
N-Boc-L-phenylalanine, 99%, Thermo Scientific Chemicals
Catalog numberA16017.14
Price (USD)/ Each
146.00
-
Chemical Identifiers
CAS13734-34-4
IUPAC Name(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-phenylpropanoic acid
Molecular FormulaC14H19NO4
InChI KeyZYJPUMXJBDHSIF-NSHDSACASA-N
SMILESCC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
Melting Point (clear melt)83.0-89.0?C
Optical Rotation24.4 ± 0.1? (C=1 in ethanol)
FormCrystals or powder or crystalline powder
N-Boc-L-phenylalanine is a derivative of Phenylalanine used in enantioselective hydrolysis of amino acid esters.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
N-Boc-L-phenylalanine is a derivative of Phenylalanine used in enantioselective hydrolysis of amino acid esters.
Solubility
Soluble in methanol, dichloromethane, dimethylformamide and N-methyl-2-pyrrolidone.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
N-Boc-L-phenylalanine is a derivative of Phenylalanine used in enantioselective hydrolysis of amino acid esters.
Solubility
Soluble in methanol, dichloromethane, dimethylformamide and N-methyl-2-pyrrolidone.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Marie Claude Fournie-Zaluski, Pascale Coric, Serge Turcaud, Luce Bruetschy, Evelyne Lucas, Florence Noble, Bernard P. Roques. Potent and systemically active aminopeptidase N inhibitors designed from active-site investigation. J. Med. Chem. 1992, 35 (7), 1259-1266.
- Sung-Hwan Moon, Yasufumi Ohfune. Efficient Syntheses of the Four Enantiomers and Diastereomers of .alpha.-Methylthreonine and Both Enantiomers of .alpha.-Methylserine. J. Am. Chem. Soc. 1994, 116 (16), 7405-7406.