(2R,2\'R)-4,4\'-Disulfanediylbis(2-aminobutanoic+acid)
Catalog Number:
(100295-302)
Supplier:
Indofine Chemical Company
Description:
Rare Organics & BioChemicals 1gm H-D-Cys(tBu)-OH. HCI 213.7 Room temperature.
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Supplier:
TCI America
Description:
CAS Number: 1676-75-1
MDL Number: MFCD00038275 Molecular Formula: C15H21NO5 Molecular Weight: 295.34 Purity/Analysis Method: >98.0% (T) Form: Crystal Melting point (°C): 86 Specific rotation [a]20/D: 21 deg (C=2, EtOH)
Catalog Number:
(F-3525.0005BA)
Supplier:
Bachem Americas
Description:
Sequence: H-D-Tyr(tBu)-allyl ester · HCl
Supplier:
Bachem Americas
Description:
Substitution 0.50-0.90 mmol/g Storage Conditions -20 +/- 5 Deg C 5g
Catalog Number:
(100279-822)
Supplier:
Indofine Chemical Company
Description:
Rare Organics & BioChemicals 1gm H-Hyp-(tBu)-OtBu. HCI 279.8 Room temperature.
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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:
Bachem Americas
Description:
LHRH is also called Gonadotropin-Releasing Hormone (GnRH) or Luteinizing Hormone-Releasing Factor (LRF).
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.
Supplier:
AMBEED, INC
Description:
H-Hyp(tBu)-OtBu.HCl, Purity: 95%, CAS Number: 367453-05-2, Appearance: Solid, Storage: Inert atmosphere, 2-8 C, Size: 1g
Catalog Number:
(102538-536)
Supplier:
Matrix Scientific
Description:
MF=C22H25NO5 MW=383.45 CAS=128107-47-1 MDL=MFCD00077071 5G
Catalog Number:
(77669-432)
Supplier:
AMBEED, INC
Description:
Z-Ser(Tos)-OMe ≥98%
Supplier:
TCI America
Description:
CAS Number: 71989-33-8
MDL Number: MFCD00037127 Molecular Formula: C22H25NO5 Molecular Weight: 383.44 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 136 Specific rotation [a]20/D: 24 deg (C=1, EtOAc)
Catalog Number:
(76804-072)
Supplier:
AMBEED, INC
Description:
(S)-2-Amino-3-(tert-butylthio)propanoic acid hydrochloride, Purity: 97%, CAS Number: 200353-65-7, Appearance: White to off-white powder or crystals, Storage: Inert atmosphere, 2-8C, Size: 5G
Supplier:
Bachem Americas
Description:
LHRH is also called Gonadotropin-Releasing Hormone (GnRH) or Luteinizing Hormone-Releasing Factor (LRF).
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-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.
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