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Fmoc-3-Ala(2-thienyl)-OH

Cat. No. M39358

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Fmoc-3-Ala(2-thienyl)-OH Structure

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Quality Control & Documentation
Biological Activity

Fmoc-3-Ala(2-thienyl)-OH is an alanine derivative.

Chemical Information
Molecular Weight 393.46
Formula C22H19NO4S
CAS Number 130309-35-2
Form Solid
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Valerie Vallet et al. Dalton Trans. Structure and dynamics of binary and ternary lanthanide(III) and actinide(III) tris[4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione] (TTA)-tributylphosphate (TBP) complexes. Part 3, the structure, thermodynamics and reaction mechanisms of 8- and 9-coordinated binary and ternary Y-TTA-TBP complexes studied by quantum chemical methods

[2] Zoltán Szabó et al. Dalton Trans. Structure and dynamics of binary and ternary lanthanide(III) and actinide(III) tris[4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione] (TTA) complexes. Part 2, the structure and dynamics of binary and ternary complexes in the Y(III)/Eu(III)-TTA-tributylphosphate (TBP) system in chloroform as studied by NMR spectroscopy

[3] Vijayakumar N Sonar et al. Acta Crystallogr C. rac-(Z)-2-(2-Thienylmethylene)-1-azabicyclo[2.2.2]octan-3-ol

[4] Kristin Kirschbaum et al. Acta Crystallogr C. The twinned crystal structure of mu-2,2'-bipyrimidine-1kappa2N1,N1':2kappa2N3,N3'-bis{tris[4,4,4-trifluoro-1-(2-thienyl)butane-1,3-dionato-kappa2O,O']terbium(III)} ethyl acetate solvate

[5] C N Hinko et al. Neuropharmacology. Anticonvulsant activity of novel derivatives of 2- and 3-piperidinecarboxylic acid in mice and rats

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Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation.

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H-Phe(2-Cl)-OH is a phenylalanine derivative.

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Fmoc-Ala-OH

Fmoc-Ala-OH is an alanine derivative.

  Catalog
Abmole Inhibitor Catalog




Keywords: Fmoc-3-Ala(2-thienyl)-OH supplier, Amino Acid Derivatives, inhibitors, activators

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