ALD00350

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-methoxy-L-phenylalanine

95% (HPLC)

• Fórmula empírica (Notação de Hill): C₂₅H₂₃NO₅
• Peso molecular: 417.45
• Número MDL: MFCD01317011
• Código UNSPSC: 12352209
• ID de substância PubChem: 329772654
• NACRES: NA.22

Propriedades

• Ensaio: 95% (HPLC)
• forma: solid
• adequação da reação: reaction type: solution phase peptide synthesis
• pf: 171-176 °C
• aplicação(ões): peptide synthesis
• temperatura de armazenamento: 2-8°C
• cadeia de caracteres SMILES: OC([C@@H](NC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)CC4=CC=CC=C4OC)=O
• InChI: 1S/C25H23NO5/c1-30-23-13-7-2-8-16(23)14-22(24(27)28)26-25(29)31-15-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-13,21-22H,14-15H2,1H3,(H,26,29)(H,27,28)/t22-/m0/s1
• chave InChI: CBCSNZJHURMDMO-QFIPXVFZSA-N

Descrição

Aplicação

Unnatrual amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835).

Outras notas

Ligand-Controlled C(sp³)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable