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| Product | Description | |
|---|---|---|
| Boc-L-Lys(Fmoc)(Me)-OH | Synonyms: Fmoc-Lys(Boc,Me)-OH; (9H-Fluoren-9-yl)MethOxy]Carbonyl Lys(Boc, Me)-OH. Grades: ≥ 98% (HPLC). CAS No. 951695-85-5. Molecular formula: C27H34N2O6. Mole weight: 482.60. |  |
| Fmoc-lys(boc)(me)-oh | Fmoc-lys(boc)(me)-oh. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fmoc-Lys(Boc)(Me)-OH;Nalpha-Fmoc-nepsiloN-metyl-nepsilon-Boc-L-lysine. Product Category: Heterocyclic Organic Compound. CAS No. 956195-85-5. Molecular formula: C27H34N2O6. Purity: 0.96. Product ID: ACM956195855. Alfa Chemistry ISO 9001:2015 Certified. Categories: 951695-85-5. |  |
| Fmoc-Lys(Boc,Me)-OH | Fmoc-Lys(Boc,Me)-OH is a lysine derivative [1]. Uses: Scientific research. Group: Peptides. CAS No. 951695-85-5. Pack Sizes: 250 mg; 1 g. Product ID: HY-66024. |  |
| Fmoc-Lys(Me, Boc)-OH | Fmoc-lys(ME,boc)-OH is a chemical compound composed of 2,2-dimethyl-4,6-dioxoheptanoic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, (S)-4-amino-6-((1,1-dimethylethoxy)carbonyl)hexanoic acid, which is commonly referred to as Fmoc-Lys(ME,Boc)-OH. This compound belongs to the family of Fmoc-amino acids, which are widely used as building blocks in peptide synthesis. Uses: Fmoc-lys(me,boc)-oh is widely used as a building block in peptide synthesis, including the synthesis of cyclic peptides, stapled peptides, and peptidomimetics. it is also used in the development of drugs and pharmaceuticals. Additional or Alternative Names: Fmoc-Lys(Me,Boc)-OH, N-α-Fmoc-N-ε-methyl-N-ε-t.-Boc-L-lysine. Product Category: Amino Acids. CAS No. 951695-85-5. Molecular formula: C27H34N2O6. Mole weight: 482.6. IUPACName: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]hexanoic acid. Canonical SMILES: CC(C)(C)OC(=O)N(C)CCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13. Density: 1.2±0.1 g/cm3. Product ID: ACM951695855. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Lys(Me,Boc)-OH | A novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS. Coupling can be carried out using any standard activation method. Removal of the Boc protecting group occurs during the course of the TFA-mediated cleavage reaction. Ref contains methods and protocols for the synthesis of arrays of histone-related peptides containing methylated arginine and lysine-residues. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-Lys(Me,Boc)-OH, N-α-Fmoc-N-ε-methyl-N-ε-t.-Boc-L-lysine. Product Category: Amino Acids. CAS No. 951695-85-5. Mole weight: 482.57. Product ID: ACM951695855-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fmoc-Lys(Me,Boc)-OH | Fmoc-Lys(Me,Boc)-OH. Group: Biochemicals. Grades: Highly Purified. CAS No. 951695-85-5. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C27H34N2O6. US Biological Life Sciences. |  Worldwide |
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