714151

Fmoc-β-叠氮-Ala-OH

≥98.0% (HPLC), for peptide synthesis

• 同義詞: (S)-3-叠氮基-2-(Fmoc-氨基)丙酸, Fmoc-3-叠氮基-L-丙氨酸
• 經驗公式（希爾表示法）: C₁₈H₁₆N₄O₄
• CAS號碼: 684270-46-0
• 分子量：: 352.34
• MDL號碼: MFCD11052919
• 分類程式碼代碼: 12352209
• PubChem物質ID: 329763258
• NACRES: NA.26

屬性

• 產品名稱: Fmoc-β-叠氮-Ala-OH, ≥98.0% (HPLC)
• 化驗: ≥98.0% (HPLC)
• 形狀: lumps
• 光學活性: [α]/D -10.0±1.0°, c = 1 in DMF
• 反應適用性: reaction type: Fmoc solid-phase peptide synthesis; reaction type: click chemistry
• 雜質: 15.3-16.5% nitrogen; 60.1-62.5% carbon
• 應用: peptide synthesis
• 官能基: Fmoc
• 儲存溫度: 2-8°C
• SMILES 字串: OC(=O)[C@H](CN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c3ccccc13
• InChI: 1S/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/m0/s1
• InChI 密鑰: ZITYCUDVCWLHPG-INIZCTEOSA-N

描述

應用

Fmoc-β-azido-Ala-OH chloride is a general N-terminal protected reagent used in the solid phase peptide synthesis. Azido group allows it to undergo copper-mediated click chemistry reactions.
It can be used in:

• Synthesis of α-N-acetylgalactosamine (α-GalNAc) linked antifreeze glycopeptides (AFGPs).
• Synthesis of stimuli-responsive multifunctional peptide gatekeepers for drug delivery applications.
• Synthesis of triazole-linked glycopeptides via Cu(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC).

包裝

Bottomless glass bottle. Contents are inside inserted fused cone.

安全資訊

• 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
• 個人防護裝備: dust mask type N95 (US), Eyeshields, Gloves