N-Fmoc-S-trityl-L-cysteine, 95%
N-Fmoc-S-trityl-L-cysteine, 95%
N-Fmoc-S-trityl-L-cysteine, 95%
Thermo Scientific Chemicals

N-Fmoc-S-trityl-L-cysteine, 95%

CAS: 103213-32-7 | C37H30NO4S | 584.71 g/mol
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Quantity:
5 g
25 g
Catalog number H27363.14
also known as H27363-14
Price (EUR)
114,00
Each
Quantity:
25 g
Request bulk or custom format
Price (EUR)
114,00
Each
Chemical Identifiers
CAS103213-32-7
SpecificationsSpecification SheetSpecification Sheet
Optical Rotation+15° to +19° (c=1 in THF)
Appearance (Color)White to pale cream
Assay (Aqueous acid-base Titration)≥94.0 to ≤106.0%
FormPowder
Melting Point (clear melt)174.0-182.0°C
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It is potentially useful for proteomics studies, and solid phase peptide synthesis techniques. Cysteine is versatile amino acid involved with many biological processes, including the formation of disulfide bonds - a critical component of protein structure. This compound could be useful as an unusual amino acid analog to aid in the deconvolution of protein structure and function.

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
It is potentially useful for proteomics studies, and solid phase peptide synthesis techniques. Cysteine is versatile amino acid involved with many biological processes, including the formation of disulfide bonds - a critical component of protein structure. This compound could be useful as an unusual amino acid analog to aid in the deconvolution of protein structure and function.

Solubility
Insoluble in water. Soluble in most organic solvents.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Laiping Xie, et al. Cellular Effects of Small Molecule PTP1B Inhibitors on Insulin Signaling.Biochemistry.,2003,42(44), 12792-12804.
  2. Shu-Li You, et al. Total synthesis of didmolamides A and B.Tetrahedron Lett.,2005,46(15), 2567-2570.