Tetraethylene+glycol+bis(p-toluenesulfonate)
Catalog Number:
(B-3915.0005BA)
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.
Supplier:
TCI America
Description:
CAS Number: 4378-13-6
MDL Number: MFCD00037766 Molecular Formula: C8H17NO3 Molecular Weight: 175.23 Purity/Analysis Method: >98.0% (T) Form: Crystal Melting point (°C): 260 Specific rotation [a]20/D: -43 deg (C=2, MeOH)
Catalog Number:
(B-4310.0005BA)
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-4325.0005BA)
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-3935.0005BA)
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:
(102541-544)
Supplier:
Matrix Scientific
Description:
MF=C23H27NO5 MW=397.48 CAS=71989-35-0 MDL=MFCD00077075 100G
Catalog Number:
(B-3925.0005BA)
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-4305.0005BA)
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.
Supplier:
TCI America
Description:
CAS Number: 71989-35-0
Molecular Formula: C23H27NO5 Molecular Weight: 397.47 Purity/Analysis Method: >98.0% (T,HPLC) Form: Crystal Melting point (°C): 133 Specific rotation [a]20/D: 15 deg (C=1, EtOAc)
Supplier:
Bachem Americas
Description:
Sequence: H-allo-Thr-OMe · HCl
Supplier:
AMBEED, INC
Description:
H-Thr(tBu)-OMe·HCl 97%
Supplier:
Bachem Americas
Description:
Sequence: Fmoc-Thr(tBu)-Wang resin (100-200 mesh)
Synonym(s): Fmoc-Thr(tBu)-p-alkoxybenzyl alcohol resin
Supplier:
Bachem Americas
Description:
Sequence: H-Thr(tBu)-OMe · HCl
Supplier:
AMBEED, INC
Description:
H-D-Thr(tBu)-OMe.HCl, Purity: 97%, CAS Number: 115141-43-0, Appearance: Colorless or white to off-white liquid or low melting solid, Storage: Inert atmosphere, Store in freezer, under -20C, Size: 1G
Supplier:
Bachem Americas
Description:
Sequence: Fmoc-Thr(tBu)-OPfp
Supplier:
Bachem Americas
Description:
Sequence: H-Thr(tBu)-2-chlorotrityl resin (200-400 mesh)
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