You Searched For: Fmoc-Pro-OH


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Supplier: Bachem Americas

Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 042043-1G , MDL Number: MFCD02094543

Supplier: Ambeed
Description: (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-2-methylpyrrolidine-2-carboxylic acid 97%

New Product

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
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: (76656-040)
Supplier: Ambeed
Description: (2S,4R)-Fmoc-4-(4-fluorobenzyl)pyrrolidine-2-carboxylic acid, Purity: 97%, CAS Number: 959576-18-2, Appearance: Solid, Storage: Sealed in dry, 2-8C, Size: 250MG


Catalog Number: (77621-998)
Supplier: Ambeed
Description: (2R,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-fluoropyrrolidine-2-carboxylic acid ≥98%

New Product


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
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: (77867-181)
Supplier: Ambeed
Description: (2R,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-fluoropyrrolidine-2-carboxylic acid ≥97%

New Product


Supplier: Ambeed
Description: (2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-methylpyrrolidine-2-carboxylic acid ≥95%

New Product

Supplier: Ambeed
Description: (2S,4R)-4-Aminopyrrolidine-2-carboxylic acid, 4-BOC, N1-FMOC protected 97%

Catalog Number: (77617-630)
Supplier: Ambeed
Description: (S)-3-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-oxo-5-(tritylamino)pentanoyl)-2,2-dimethyloxazolidine-4-carboxylic acid ≥97%

New Product


Catalog Number: (77622-712)
Supplier: Ambeed
Description: (4S,5R)-3-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid ≥95%

New Product


Catalog Number: (77569-270)
Supplier: Ambeed
Description: (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4,4-difluoropyrrolidine-2-carboxylic acid 96%

New Product


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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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 call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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