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Boc-N-Me-D-Tyr-OH\u00B7DCHA
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Boc-N-Me-D-Tyr-OH\u00B7DCHA
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042079-5G , MDL Number: MFCD00153314
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042426-1G , MDL Number: MFCD00236864
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041899-1G , MDL Number: MFCD02682284
Supplier:
TCI America
Description:
CAS Number: 47375-34-8
MDL Number: MFCD00065598 Molecular Formula: C18H27NO5 Molecular Weight: 337.42 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 117 Specific rotation [a]20/D: -16 deg (C=1, DMF) Storage Temperature: 0-10°C
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042438-5G , MDL Number: MFCD00038522
Catalog Number:
(A-4210.0001BA)
Supplier:
Bachem Americas
Description:
Sequence: Boc-β-tBu-D-Ala-OH
Supplier:
Thermo Scientific Chemicals
Description:
250mg CAS: 51293-47-1, MDL: MFCD00153314
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041912-5G , MDL Number: MFCD00065601
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042082-1G , MDL Number: MFCD02682605
Supplier:
AMBEED, INC
Description:
(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-fluoro-4-hydroxyphenyl)propanoic acid 95%
Catalog Number:
(101855-764)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042428-5G , MDL Number: MFCD00063137
Catalog Number:
(B-4315.0005BA)
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:
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-ethoxyphenyl)propanoic acid 97%
Catalog Number:
(76985-272)
Supplier:
AMBEED, INC
Description:
Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate, Purity: 95%, CAS number: 69912-63-6, Appearance: White to off-white powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G
Supplier:
AMBEED, INC
Description:
(2S,4S)-1-(tert-Butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylic acid 98%
Catalog Number:
(B-3930.0005BA)
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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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
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