You Searched For: Fmoc-L-allo-threoninol


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Supplier: Bachem Americas
Description: Sequence: Fmoc-Glu(OtBu)-OPfp

Catalog Number: (B-2025.0001BA)
Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Cys(Trt)-OPfp


Supplier: Bachem Americas
Description: Fmoc-Tyr(SO₃nP), a protected derivative of sulfotyrosine. The neopentyl ester is stable under the conditions of Fmoc-SPPS including the TFA-cleavage, but can be removed by treatment with aqueous ammonium acetate or sodium acetate. Thus, premature loss of sulfate groups during the final deprotection is prevented.

Supplier: Bachem Americas
Description: Protected derivative of L-azidohomoalanine (Aha), a Met isostere. This building block for 'click chemistry' additionally creates a specific cleavage site in peptides, Aha-containing sequences can be cleaved under mild conditions in the presence of phosphines or dithiols via formation of homoserine lactone.

Supplier: Bachem Americas
Description: Sequence: Fmoc-Orn(Boc)-OH

Supplier: Thermo Scientific Chemicals
Description: 2-(Fmoc-amino)benzoic acid, 98%
Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Asp(OtBu)-OH

Supplier: Bachem Americas
Description: Sequence: Z-Lys(Fmoc)-OH

Supplier: Bachem Americas
Description: Sequence: Fmoc-Glu(OSu)-OtBu

Supplier: TCI America
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-(2-furyl)-L-alanine, Purity: >98.0%(T), CAS Number: 159611-02-6, MF: C22H19NO5, MW: 377.4, Synonym: N-Fmoc-3-(2-furyl)-L-alanine, Fmoc-B-(2-furyl)-Ala-OH, Form: Crystal- Powder, Size: 200MG

SDS

Supplier: Bachem Americas
Description: Sequence: Fmoc-Cys(Trt)-OPfp

Supplier: Thermo Scientific Chemicals
Description: Base sensitive amino protecting group for solid-phase peptide synthesis
Supplier: Bachem Americas
Description: Sequence: Fmoc-Asp(OtBu)-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.

Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Lys(Boc)-OH

Supplier: TCI America
Description: 9-[(9H-Fluoren-9-ylmethoxy)carbonylamino]-4,7-dioxanonanoic Acid, Purity: >98.0%(HPLC)(T), CAS: 872679-70-4, MF: C22H25NO6, MW: 399.44, Synonym: 9-(Fmoc-amino)-4,7-dioxanonanoic Acid, Fmoc-NH-PEG2-CH2CH2COOH, Size: 200MG
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