You Searched For: Fmoc-N-Me-Phe-OH


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Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Tyr(Et)-OH

Supplier: Bachem Americas
Description: Fmoc-Phe(D₅)-OH was N-methylated and used in the synthesis of an internal standard for the quantification of the μ-opioid receptor antagonist DAMGO (H-2535) in ovine plasma samples by MALDI-TOF-MS.

Supplier: Bachem Americas
Description: Sequence: Fmoc-Arg(Me)₂-OH (symmetrical)

Catalog Number: (TCF1028-1G)
Supplier: TCI America
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-leucine, Purity: >98.0%(HPLC)(T), CAS number: 103478-62-2, Molecular Formula: C22H25NO4, Molecular Weight: 367.45, Synonym: Fmoc-N-Me-Leu-OH, N-Fmoc-N-methyl-L-leucine, Size: 1G


Supplier: TCI America
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-norvaline, Purity: >98.0%(HPLC)(T), CAS number: 252049-05-1, Molecular Formula: C21H23NO4, Molecular Weight: 353.42, Synonym: Fmoc-N-Me-Nva-OH, N-Fmoc-N-methyl-L-norvaline, Size: 5G

Supplier: Bachem Americas
Description: Sequence: Fmoc-p-nitro-Phe-OH

Supplier: Bachem Americas
Description: Sequence: Fmoc-N-Me-Ala-OH

Supplier: Bachem Americas
Description: For Fmoc-dipeptides Fmoc-Xaa-Gly-OH and Fmoc-Xaa-Pro-OH, which can be used as building blocks in Fmoc-SPPS, please see also the subfamily 'Fmoc-Dipeptide Building Blocks' in the 'Amino Acid Derivatives' section. Pseudoproline dipeptides and isoacyl dipeptides can be found in this section as well. In case of a strong tendency towards diketopiperazine formation during Fmoc-SPPS, Fmoc-dipeptides have been coupled even at the risk of a some epimerization.

Supplier: Bachem Americas

Supplier: Bachem Americas
Description: Derivative of a stable sulfotyrosine mimic suitable for Fmoc-SPPS. The lateral trichloroethyl (Tce) group is cleaved by hydrogenolysis (H₂/Pd in the presence of ammonium formate).

Supplier: Bachem Americas
Description: Bachem additionally offers deuterated phenylalanine: Fmoc-[ring-D₅]Phe-OH B-4115.

Supplier: TCI America
Description: CAS Number: 86123-10-6
MDL Number: MFCD00062955
Molecular Formula: C24H21NO4
Molecular Weight: 387.44
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Melting point (°C): 183
Specific rotation [a]20/D: 38 deg (C=1, DMF)
Catalog Number: (AAH63411-06)
Supplier: Thermo Scientific Chemicals
Description: N-Fmoc-N-methyl-L-alanine, 95%

Supplier: Bachem Americas
Description: For Fmoc-dipeptides Fmoc-Xaa-Gly-OH and Fmoc-Xaa-Pro-OH, which can be used as building blocks in Fmoc-SPPS, please see also the subfamily 'Fmoc-Dipeptide Building Blocks' in the 'Amino Acid Derivatives' section. Pseudoproline dipeptides and isoacyl dipeptides can be found in this section as well. In case of a strong tendency towards diketopiperazine formation during Fmoc-SPPS, Fmoc-dipeptides have been coupled even at the risk of a some epimerization.

Catalog Number: (B-4100.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Catalog Number: (B-4085.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


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