132327-80-1
132327-80-1
Chemical Structure
Fmoc-Gln(Trt)-OH
- CAS No.: 132327-80-1
- Formula:C39H34N2O5
- Molecular Weight:610.70
IUPAC Name: N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N5-trityl-L-glutamine
InChIKey: WDGICUODAOGOMO-DHUJRADRSA-N
SMILES: O=C(CC[C@H](NC(OCC1C2=C(C=CC=C2)C3=C1C=CC=C3)=O)C(O)=O)NC(C4=CC=CC=C4)(C5=CC=CC=C5)C6=CC=CC=C6
Biological Activity: Fmoc-Gln(Trt)-OH is a glutamine derivative containing amine protecting group Fmoc. Fmoc-Gln(Trt)-OH can be used in solid-phase peptide synthesis[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fmoc-Gln(Trt)-OH | 99.86% | Fmoc-Gln(Trt)-OH is a glutamine derivative containing amine protecting group Fmoc. Fmoc-Gln(Trt)-OH can be used in solid-phase peptide synthesis. | ||||||||||||||||||||
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Fmoc-Gln(Trt)-OH-13C5,15N2 | Fmoc-Gln(Trt)-OH-13C5,15N2 is the 13C-labeled and 15N-labeled Fmoc-Gln(Trt)-OH (HY-W013081). Fmoc-Gln(Trt)-OH is a glutamine derivative containing amine protecting group Fmoc. Fmoc-Gln(Trt)-OH can be used in solid-phase peptide synthesis. | |||||||||||||||||||||
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References
- [1]. Carey RI, et al. Protection of asparagine and glutamine during N alpha-Bpoc-based solid-phase peptide synthesis. Int J Pept Protein Res. 1996 Mar;47(3):209-13. [Content Brief]
- [2]. Alewood P, et al. [2] Rapid in situ neutralization protocols for Boc and Fmoc solid-phase chemistries. Methods in enzymology, 1997, 289: 14-29.
