15408

N-叔丁氧羰基-1,3-丙二胺

≥97.0% (GC/NT)

• 同義詞: N-(3-氨基丙基)氨基甲酸叔丁酯, N-Boc-1,3-二氨基丙烷
• 線性公式: (CH₃)₃COCONH(CH₂)₃NH₂
• CAS號碼: 75178-96-0
• 分子量：: 174.24
• Beilstein: 3588328
• MDL號碼: MFCD00210021
• 分類程式碼代碼: 12352116
• PubChem物質ID: 57647415
• NACRES: NA.22

屬性

• 品質等級: 100
• 化驗: ≥97.0% (GC/NT)
• 反應適用性: reagent type: cross-linking reagent
• 折射率: n20/D 1.454 (lit.); n20/D 1.459
• bp: 203 °C (lit.)
• mp: 22 °C (lit.)
• 密度: 0.998 g/mL at 20 °C (lit.)
• 官能基: Boc; amine
• SMILES 字串: NCCCNC(OC(C)(C)C)=O
• InChI: 1S/C8H18N2O2/c1-8(2,3)12-7(11)10-6-4-5-9/h4-6,9H2,1-3H3,(H,10,11)
• InChI 密鑰: POHWAQLZBIMPRN-UHFFFAOYSA-N

描述

應用

• Tackling vancomycin-resistant bacteria with ′lipophilic–vancomycin–carbohydrate conjugates′: This study discusses the synthesis of derivatives using N-Boc-1,3-propanediamine to develop new antibacterial agents targeting resistant bacterial strains (Yarlagadda et al., 2015).
• Sulfonamides differing in the alkylamino substituent length–Synthesis, electrochemical characteristic, acid-base profile and complexation properties: The study involves N-Boc-1,3-propanediamine in the synthesis of novel sulfonamide derivatives with potential biochemical applications (Ciesielska et al., 2022).
• Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics: Research demonstrating selective α-alkylation of N-Boc-1,3-propanediamine, highlighting a novel method in organic synthesis (Ye et al., 2018).

其他說明

合成亚精胺类似物；制备药理活性化合物。

安全資訊

• 象形圖: GHS05,GHS07
• 訊號詞: Danger
• 危險聲明: H302,H314
• 防範說明: P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363
• 危險分類: Acute Tox. 4 Oral - Skin Corr. 1B
• 儲存類別代碼: 8A - Combustible corrosive hazardous materials
• 水污染物質分類（WGK）: WGK 3
• 閃點（°F）: 228.2 °F - closed cup
• 閃點（°C）: 109 °C - closed cup
• 個人防護裝備: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter