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| Product | Description | |
|---|---|---|
| Fmoc-Asn(Trt)-OH | Fmoc-Asn(Trt)-OH. Group: Biochemicals. Alternative Names: N-Alpha-Fmoc-N-beta-trityl-L-asparagine; Fmoc-Asn(Trt)-OH. Grades: Highly Purified. CAS No. 132388-59-1. Pack Sizes: 25g, 50g, 100g, 250g. Molecular Formula: C38H32N2O5, Molecular Weight: 596.67. US Biological Life Sciences. |  Worldwide |
| Fmoc-Asn(Trt)-OH | Fmoc-Asn(Trt)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Fmoc-Asn(Trt)-OH can be used for synthesis of Fmoc-based solid-phase peptide synthesis [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 132388-59-1. Pack Sizes: 10 mM * 1 mL; 25 g. Product ID: HY-W002327. |  |
| FMOC-Asn(Trt)-OH | High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Fmoc-Asn(Trt)-OH has good solubility properties in most organic solvents, and its use has been shown to result in significantly purer peptides than other derivatives used for the introduction of Asn. Coupling can be performed by standard procedures. The trityl group is normally removed by 95% TFA in 1-3 hours, with no alkylation of Trp residues. When Asn(Trt) is the N-terminal residue, the reaction time may need to be extended to ensure complete deprotection. Literature references P. Sieber, et al. in 'Innovation & Perspectives in Solid Phase Synthesis, 1st International Symposium', R. Epton (Eds), SPCC UK Ltd., Birmingham, 1990, pp. 577. P. Sieber, et al. (1991) Tetrahedron Lett., 32, 739. M. Friede, et al. (1992) Pept. Res., 5, 145. Uses: Fmoc-asn(trt)-oh has diverse applications in scientific experiments. it is commonly used in peptide synthesis, where it is used as a building block to assemble longer peptides. other applications include generating specific peptide sequences for biological studies, designing new drugs, and studying protein interactions. Additional or Alternative Names: FMOC-Asn(Trt)-OH, N-α-Fmoc-N-β-trityl-L-asparagine. Product Category: Amino Acids. CAS No. 132388-59-1. Molecular formula: C38H32N2O5. Mole weight: 596.67. Cano |  |
| Fmoc-Asn(Trt)-OH-15N2 | Fmoc-Asn(Trt)-OH-15N2. Uses: Peptide synthesis. Product Category: Amino Acids. CAS No. 204633-98-7. Molecular formula: Trt-15NHCOCH2CH(15NH-Fmoc)CO2H. Mole weight: 598.66. Canonical SMILES: OC(=O)[C@H](CC(=O)[15NH]C(c1ccccc1)(c2ccccc2)c3ccccc3)[15NH]C(=O)OCC4c5ccccc5-c6ccccc46. Product ID: ACM204633987-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Asn(Trt)-Gly-OH | Synonyms: N-(fluorenylmethoxycarbonyl)-N4-trityl-L-asparagyl-glycine; N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-beta-trityl-L-asparaginyl-glycine; Glycine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-(triphenylmethyl)-L-asparaginyl-; N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-trityl-L-asparaginylglycine. Grades: ≥95% by HPLC. CAS No. 1260093-07-9. Molecular formula: C40H35N3O6. Mole weight: 653.72. |  |
| Fmoc-Asn(Trt)-Ser(psiMe,Mepro)-OH | This pseudoproline dipeptide is undoubtedly the most effective and simplest to use tool for overcoming aggregation and enhancing peptide quality in Fmoc SPPS for peptide containing the Asn-Ser dipeptide motif. It consists of a dipeptide in which the serine residue has been reversibly protected as a structure-breaking proline-like TFA-labile oxazolidine. The reason pseudoproline residue is introduced as a dipeptide is because it avoids the need to acylate the hindered oxazolidine nitrogen. This has the added advantage of extending the peptide chain by two residues in one step. The serine residue is regenerated during the normal TFA-mediated cleavage reaction. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-Asn(Trt)-Ser(psiMe,Mepro)-OH. Product Category: Amino Acids. CAS No. 920519-33-1. Mole weight: 723.81. Product ID: ACM920519331-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Asn(Trt)-Ser[Psi(Me,Me)Pro]-OH | Synonyms: Fmoc-Asn(Trt)-Ser[Ψ(Me,Me)Pro]-OH; (S)-3-[Na-(9-Fluorenylmethyloxycarbonyl)-Na-trityl-L-asparaginyl]-2,2-dimethyloxazolidine-4-carboxylic acid; 3-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-(tritylamino)butanoyl]-2,2-dimethyl-1,3-oxazolidine-4-carboxylic acid; 6787AH; Fmoc-L-Asn(Trt)-L-Ser(Psi(Me,Me)pro)-OH. Grades: ≥ 99% (HPLC). CAS No. 920519-33-1. Molecular formula: C44H41N3O7. Mole weight: 723.82. | |
| Fmoc-Asn(Trt)-Ser[Psi(Me,Me)Pro]-OH 98+% (HPLC) | Fmoc-Asn(Trt)-Ser[Psi(Me,Me)Pro]-OH 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 920519-33-1. Pack Sizes: 1g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Fmoc-Asn(Trt)-Thr[Psi(Me,Me)Pro]-OH | Synonyms: Fmoc-Asn(Trt)-Thr(ΨMe,Mepro)-OH; (4S,5R)-3-[Nα-(9-Fluorenylmethyloxycarbonyl)-Nβ-trityl-L-asparaginyl]-2,2,5-trimethyloxazolidine-4-carboxylic acid; 4-Oxazolidinecarboxylic acid, 3-[(2S)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1,4-dioxo-4-[(triphenylmethyl)amino]butyl]-2,2,5-trimethyl-, (5R)-; (5R)-3-(N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N4-trityl-L-asparaginyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid; Fmoc-Asn(Trt)-Thr(Psime,Mepro)-OH; Fmoc-L-Asn(Trt)-L-Thr(Psi(Me,Me)pro)-OH. Grades: ≥ 96% (HPLC). CAS No. 957780-59-5. Molecular formula: C45H43N3O7. Mole weight: 737.84. | |
| Fmoc-Asn(Trt)-Thr[Psi(Me,Me)Pro]-OH ≥96% (HPLC) | Fmoc-Asn(Trt)-Thr[Psi(Me,Me)Pro]-OH ≥96% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 957780-59-5. Pack Sizes: 1g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Fmoc-Asn(Trt)-Thr(yMe,Mepro)-OH | Fmoc-Asn(Trt)-Thr(yMe,Mepro)-OH. Group: Biochemicals. Grades: Highly Purified. CAS No. 957780-59-5. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Fmoc-Asn(Dmcp)-OH | A superior derivative to Fmoc-Asn(Trt)-OH for the synthesis of Asn-containing peptides by Fmoc SPPS. Fmoc-Asn(Dmcp)-OH is more soluble in DMF than Fmoc-Asn(Trt)-OH, thereby facilitating coupling reactions at higher concentration. Cleavage of the Dmcp group is rapid, even when the residue is located at the N-terminus of a peptide. Coupling of Dmcp-protected derivatives is faster than that of the corresponding hindered Trt derivatives. Dmcp-protected peptides have enhanced solubility. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-Asn(Dmcp)-OH, N-α-Fmoc-N-β-(1-cyclopropyl-1-methylethyl)-L-asparagine. Product Category: Amino Acids. CAS No. 172947-19-2. Mole weight: 436.5. Product ID: ACM172947192. Alfa Chemistry ISO 9001:2015 Certified. | |
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