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Thermo Scientific Chemicals
N-Fmoc-N-methyl-D-leucine, 97%
CAS: 103478-63-3 | C22H25NO4 | 367.45 g/mol
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Catalog number H63895.14
also known as H63895-14
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Quantity:
25 g
Chemical Identifiers
CAS103478-63-3
IUPAC Name(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)-4-methylpentanoic acid
Molecular FormulaC22H25NO4
InChI KeyBUJQSIPFDWLNDC-GNLPSFAGNA-N
SMILESCC(C)C[C@@H](N(C)C(=O)OCC1C2=CC=CC=C2C2=CC=CC=C12)C(O)=O
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Specifications
Specification Sheet
Specification SheetMelting Point110-120?C
Optical Rotation+19? to +25? (c=1 in DMF)
Assay (HPLC)≥96.0%
Tripeptides were prepared by means of coupling of N-Fmoc-N-methyl-D-leucine.
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
Tripeptides were prepared by means of coupling of N-Fmoc-N-methyl-D-leucine.
Solubility
Soluble in clear solution (0.3 gram in 2 ml DMF).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, heat.
Tripeptides were prepared by means of coupling of N-Fmoc-N-methyl-D-leucine.
Solubility
Soluble in clear solution (0.3 gram in 2 ml DMF).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, heat.
RUO – Research Use Only
Shinichiro Fuse,; Yuto Mifune,; Takashi Takahashi. Efficient Amide Bond Formation through a Rapid and Strong Activation of Carboxylic Acids in a Microflow Reactor. Angew. Chem. Int. Ed 2014, 53 851 -855.