Print…

You Searched For: Fmoc-Phe-OSu


12,125  results were found

Refine Results Sort by
SearchResultCount:"12125"

Sort Results

List View Easy View

Rate These Search Results

Image Unavailable-AAH51962-06

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine 98%

Supplier: Thermo Scientific Chemicals
Description: 1g CAS: 95753-55-2, MDL: MFCD00057810

SDS Certificates

Image Unavailable-77549-794

(S)-11-Benzyl-1-(9H-fluoren-9-yl)-3,6,9,12,15-pentaoxo-2,18-dioxa-4,7,10,13,16-pentaazaicosan-20-oic acid ≥95%

Supplier: Ambeed
Description: (S)-11-Benzyl-1-(9H-fluoren-9-yl)-3,6,9,12,15-pentaoxo-2,18-dioxa-4,7,10,13,16-pentaazaicosan-20-oic acid ≥95%

New Product

Image Unavailable-B-3920.0005BA

Fmoc-Phe-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-3920.0005BA)
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.
Image Unavailable-77146-680

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,5-dichlorophenyl)propanoic acid 97%

Supplier: Ambeed
Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,5-dichlorophenyl)propanoic acid 97%

Image Unavailable-TCF0443-5G

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 95753-55-2
MDL Number: MFCD00057810
Molecular Formula: C24H20N2O6
Molecular Weight: 432.43
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -40 deg (C=1, DMF)

SDS

Image Unavailable-B-1495.0005BA

Fmoc-Gly-Phe-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.

Image Unavailable-101914-328

2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-fluorophenyl)propanoic acid ≥95%

Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 058233-500MG , MDL Number: MFCD00237667

Image Unavailable-77892-399

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid 98%

Catalog Number: (77892-399)
Supplier: Ambeed
Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid 98%

New Product


Product Image-77866-505

(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylbutanoic acid 97%

Supplier: Ambeed
Description: (2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylbutanoic acid 97%

New Product

Image Unavailable-TCF0900-1G

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]pentafluoro-L-phenylalanine ≥97.0% (by HPLC, titration analysis)

Catalog Number: (TCF0900-1G)
Supplier: TCI America
Description: CAS Number: 205526-32-5
MDL Number: MFCD00270612
Molecular Formula: C24H16F5NO4
Molecular Weight: 477.39
Purity/Analysis Method: >97.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -19 deg (C=1, MeOH)
Storage Temperature: 0-10°C

SDS


Image Unavailable-77886-111

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-dimethylphenyl)propanoic acid ≥98%

Supplier: Ambeed
Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-dimethylphenyl)propanoic acid ≥98%

New Product

Image Unavailable-76979-546

(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-chlorophenyl)propanoic acid 95%

Supplier: Ambeed
Description: (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-chlorophenyl)propanoic acid, Purity: 95%, CAS number: 479064-92-1, Appearance: White to off-white powder or crystals, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1G

Image Unavailable-77874-859

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(tert-butoxycarbonyl)phenyl)propanoic acid ≥98%

Catalog Number: (77874-859)
Supplier: Ambeed
Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(tert-butoxycarbonyl)phenyl)propanoic acid ≥98%

New Product


Image Unavailable-77112-840

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid 95%

Catalog Number: (77112-840)
Supplier: Ambeed
Description: (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid, Purity: 95%, CAS Number: 1217820-78-4, Appearance: White to off-white powder or crystals, Storage: Sealed in dry, 2-8 deg C, Size: 250mg
Image Unavailable-D-2200.0025BA

Tricyclic amide linker resin (DL-form) 200-400 mesh

Supplier: Bachem Americas
Description: Ramage resin is highly suitable for the preparation of peptide amides by the Fmoc-strategy and is recommended for C-terminal Phe, Tyr and Ile. Cleavage has been performed with 50 % TFA in CH₂Cl₂ or 95% aqueous TFA. Scavengers may be required. Tricyclic amide linker resin has been used for the synthesis of fluorogenic substrates for continuous assay of aminopeptidase P. Bachem additionally offers the Ramage amide linker (Q-2745) to be coupled to other types of carrier resin.

Image Unavailable-B-4300.0005BA

Fmoc-Phe-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4300.0005BA)
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.
Inquire for Price
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.
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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
241 - 256 of 12,125
no targeter for Bottom