ALD00352

Boc-2-methoxy-L-phenylalanine

97%

• 别名: (S)-2-(tert-butoxycarbonylamino)-3-(2-methoxyphenyl)propanoic acid
• 经验公式（希尔记法）: C₁₅H₂₁NO₅
• CAS号: 143415-63-8
• 分子量: 295.33
• MDL號碼: MFCD01860640
• 分類程式碼代碼: 12352209
• PubChem物質ID: 329772655
• NACRES: NA.22

属性

• 化驗: 97%
• 形狀: powder
• 反應適用性: reaction type: Boc solid-phase peptide synthesis; reagent type: ligand; reaction type: C-H Activation
• mp: 157 °C
• 應用: peptide synthesis
• 儲存溫度: 2-8°C
• SMILES 字串: OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O
• InChI: 1S/C15H21NO5/c1-15(2,3)21-14(19)16-11(13(17)18)9-10-7-5-6-8-12(10)20-4/h5-8,11H,9H2,1-4H3,(H,16,19)(H,17,18)/t11-/m0/s1
• InChI 密鑰: QMHKMTAKTUUKEK-NSHDSACASA-N

说明

應用

Unnatural 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).

其他說明

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

安全信息

• 儲存類別代碼: 11 - Combustible Solids
• 水污染物質分類（WGK）: WGK 3
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable